Linked Data
ClinVar Variation Id:
1051676
ClinVar RCV Id:
RCV001359746
dbSNP Id:
rs763457920
ExAC:
16:10995895 C / G
gnomAD v2:
16-10995895-C-G
gnomAD v3:
16-10902038-C-G
gnomAD v4:
16-10902038-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.10902038C>G , CM000678.2:g.10902038C>G | GRCh38 |
| NC_000016.9:g.10995895C>G , CM000678.1:g.10995895C>G | GRCh37 |
| NC_000016.8:g.10903396C>G | NCBI36 |
| NG_009628.1:g.29841C>G , LRG_49:g.29841C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695879.1:n.507C>G | ||
| ENST00000324288.14:c.482C>G MANE Select | ENSP00000316328.8:p.Ala161Gly | |
| ENST00000637439.1:c.716C>G | ENSP00000489907.1:p.Ala239Gly | |
| ENST00000324288.12:c.482C>G | ENSP00000316328.8:p.Ala161Gly | |
| ENST00000381835.9:c.481+480C>G | ENSP00000371257.5:n.481+480C>G | |
| ENST00000537380.1:n.482C>G | ||
| ENST00000570546.5:n.603C>G | ||
| ENST00000571186.5:c.*203C>G | ENSP00000459829.1:n.*203C>G | |
| ENST00000573309.5:n.599+480C>G | ||
| ENST00000576601.1:c.410C>G | ENSP00000459608.1:p.Ala137Gly | |
| ENST00000611587.4:c.484+480C>G | ENSP00000483487.1:n.484+480C>G | |
| ENST00000618207.4:c.482C>G | ENSP00000484761.1:p.Ala161Gly | |
| ENST00000618327.4:c.485C>G | ENSP00000485010.1:p.Ala162Gly | |
| NM_000246.3:c.482C>G , LRG_49t1:c.482C>G | NP_000237.2:p.Ala161Gly | |
| NM_001286402.1:c.485C>G | NP_001273331.1:p.Ala162Gly | |
| NM_001286403.1:c.481+480C>G | NP_001273332.1:n.481+480C>G | |
| NR_104444.1:n.615C>G | ||
| XM_006720880.2:c.779C>G | XP_006720943.2:p.Ala260Gly | |
| XM_011522484.1:c.779C>G | XP_011520786.1:p.Ala260Gly | |
| XM_011522485.1:c.779C>G | XP_011520787.1:p.Ala260Gly | |
| XM_011522486.1:c.779C>G | XP_011520788.1:p.Ala260Gly | |
| XM_011522487.1:c.679+480C>G | XP_011520789.1:n.679+480C>G | |
| XM_011522488.1:c.530C>G | XP_011520790.1:p.Ala177Gly | |
| XM_011522489.1:c.676+480C>G | XP_011520791.1:n.676+480C>G | |
| XM_011522490.1:c.527C>G | XP_011520792.1:p.Ala176Gly | |
| XM_011522491.1:c.779C>G | XP_011520793.1:p.Ala260Gly | |
| XM_011522492.1:c.485C>G | XP_011520794.1:p.Ala162Gly | |
| XM_011522493.1:c.482C>G | XP_011520795.1:p.Ala161Gly | |
| XM_011522494.1:c.413C>G | XP_011520796.1:p.Ala138Gly | |
| XM_011522495.1:c.484+480C>G | XP_011520797.1:n.484+480C>G | |
| XM_011522496.1:c.481+480C>G | XP_011520798.1:n.481+480C>G | |
| XR_932841.1:n.794C>G | ||
| XR_932842.1:n.794C>G | ||
| XR_932843.1:n.794C>G | ||
| XR_932846.1:n.794C>G | ||
| XR_932847.1:n.794C>G | ||
| XR_932848.1:n.631+480C>G | ||
| XM_006720880.3:c.779C>G | XP_006720943.2:p.Ala260Gly | |
| XM_011522484.3:c.779C>G | XP_011520786.1:p.Ala260Gly | |
| XM_011522485.2:c.779C>G | XP_011520787.1:p.Ala260Gly | |
| XM_011522486.2:c.779C>G | XP_011520788.1:p.Ala260Gly | |
| XM_011522487.2:c.679+480C>G | XP_011520789.1:n.679+480C>G | |
| XM_011522488.2:c.530C>G | XP_011520790.1:p.Ala177Gly | |
| XM_011522489.2:c.676+480C>G | XP_011520791.1:n.676+480C>G | |
| XM_011522490.2:c.527C>G | XP_011520792.1:p.Ala176Gly | |
| XM_011522491.2:c.779C>G | XP_011520793.1:p.Ala260Gly | |
| XM_011522492.2:c.485C>G | XP_011520794.1:p.Ala162Gly | |
| XM_011522493.2:c.482C>G | XP_011520795.1:p.Ala161Gly | |
| XM_011522494.2:c.413C>G | XP_011520796.1:p.Ala138Gly | |
| XM_011522495.2:c.484+480C>G | XP_011520797.1:n.484+480C>G | |
| XM_011522496.2:c.481+480C>G | XP_011520798.1:n.481+480C>G | |
| XM_024450280.1:c.725C>G | XP_024306048.1:p.Ala242Gly | |
| XM_024450281.1:c.724+480C>G | XP_024306049.1:n.724+480C>G | |
| XR_001751904.1:n.798C>G | ||
| XR_932841.3:n.796C>G | ||
| XR_932842.2:n.796C>G | ||
| XR_932846.3:n.798C>G | ||
| XR_932847.3:n.798C>G | ||
| NM_001286403.2:c.481+480C>G | NP_001273332.1:n.481+480C>G | |
| NR_104444.2:n.611C>G | ||
| NM_000246.4:c.482C>G MANE Select | NP_000237.2:p.Ala161Gly | |
| NM_001379330.1:c.484+480C>G | NP_001366259.1:n.484+480C>G | |
| NM_001379331.1:c.481+480C>G | NP_001366260.1:n.481+480C>G | |
| NM_001379332.1:c.485C>G | NP_001366261.1:p.Ala162Gly | |
| NM_001379333.1:c.482C>G | NP_001366262.1:p.Ala161Gly | |
| NM_001379334.1:c.413C>G | NP_001366263.1:p.Ala138Gly |