Linked Data
ClinVar Variation Id:
317695
ClinVar RCV Id:
RCV000283889
dbSNP Id:
rs201215476
ExAC:
16:11000867 G / A
gnomAD v2:
16-11000867-G-A
gnomAD v3:
16-10907010-G-A
gnomAD v4:
16-10907010-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.10907010G>A , CM000678.2:g.10907010G>A | GRCh38 |
| NC_000016.9:g.11000867G>A , CM000678.1:g.11000867G>A | GRCh37 |
| NC_000016.8:g.10908368G>A | NCBI36 |
| NG_009628.1:g.34813G>A , LRG_49:g.34813G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695879.1:n.1412G>A | ||
| ENST00000324288.14:c.1518G>A MANE Select | ENSP00000316328.8:p.Ala506= | |
| ENST00000324288.12:c.1518G>A | ENSP00000316328.8:p.Ala506= | |
| ENST00000381835.9:c.860-1973G>A | ENSP00000371257.5:n.860-1973G>A | |
| ENST00000537380.1:n.1006+2198G>A | ||
| ENST00000570546.5:n.1639G>A | ||
| ENST00000573309.5:n.1489G>A | ||
| ENST00000611587.4:c.1374G>A | ENSP00000483487.1:p.Ala458= | |
| ENST00000618207.4:c.1006+2198G>A | ENSP00000484761.1:n.1006+2198G>A | |
| ENST00000618327.4:c.1521G>A | ENSP00000485010.1:p.Ala507= | |
| NM_000246.3:c.1518G>A , LRG_49t1:c.1518G>A | NP_000237.2:p.Ala506= | |
| NM_001286402.1:c.1521G>A | NP_001273331.1:p.Ala507= | |
| NM_001286403.1:c.860-1973G>A | NP_001273332.1:n.860-1973G>A | |
| NR_104444.1:n.1139+2198G>A | ||
| XM_006720880.2:c.1815G>A | XP_006720943.2:p.Ala605= | |
| XM_011522484.1:c.1815G>A | XP_011520786.1:p.Ala605= | |
| XM_011522485.1:c.1815G>A | XP_011520787.1:p.Ala605= | |
| XM_011522486.1:c.1815G>A | XP_011520788.1:p.Ala605= | |
| XM_011522487.1:c.1569G>A | XP_011520789.1:p.Ala523= | |
| XM_011522488.1:c.1566G>A | XP_011520790.1:p.Ala522= | |
| XM_011522489.1:c.1566G>A | XP_011520791.1:p.Ala522= | |
| XM_011522490.1:c.1563G>A | XP_011520792.1:p.Ala521= | |
| XM_011522491.1:c.1815G>A | XP_011520793.1:p.Ala605= | |
| XM_011522492.1:c.1521G>A | XP_011520794.1:p.Ala507= | |
| XM_011522493.1:c.1518G>A | XP_011520795.1:p.Ala506= | |
| XM_011522494.1:c.1449G>A | XP_011520796.1:p.Ala483= | |
| XM_011522495.1:c.1374G>A | XP_011520797.1:p.Ala458= | |
| XM_011522496.1:c.1371G>A | XP_011520798.1:p.Ala457= | |
| XR_932841.1:n.1830G>A | ||
| XR_932842.1:n.1830G>A | ||
| XR_932843.1:n.1830G>A | ||
| XR_932846.1:n.1830G>A | ||
| XR_932847.1:n.1830G>A | ||
| XR_932848.1:n.1010-1973G>A | ||
| XM_006720880.3:c.1815G>A | XP_006720943.2:p.Ala605= | |
| XM_011522484.3:c.1815G>A | XP_011520786.1:p.Ala605= | |
| XM_011522485.2:c.1815G>A | XP_011520787.1:p.Ala605= | |
| XM_011522486.2:c.1815G>A | XP_011520788.1:p.Ala605= | |
| XM_011522487.2:c.1569G>A | XP_011520789.1:p.Ala523= | |
| XM_011522488.2:c.1566G>A | XP_011520790.1:p.Ala522= | |
| XM_011522489.2:c.1566G>A | XP_011520791.1:p.Ala522= | |
| XM_011522490.2:c.1563G>A | XP_011520792.1:p.Ala521= | |
| XM_011522491.2:c.1815G>A | XP_011520793.1:p.Ala605= | |
| XM_011522492.2:c.1521G>A | XP_011520794.1:p.Ala507= | |
| XM_011522493.2:c.1518G>A | XP_011520795.1:p.Ala506= | |
| XM_011522494.2:c.1449G>A | XP_011520796.1:p.Ala483= | |
| XM_011522495.2:c.1374G>A | XP_011520797.1:p.Ala458= | |
| XM_011522496.2:c.1371G>A | XP_011520798.1:p.Ala457= | |
| XM_024450280.1:c.1761G>A | XP_024306048.1:p.Ala587= | |
| XM_024450281.1:c.1614G>A | XP_024306049.1:p.Ala538= | |
| XR_001751904.1:n.1834G>A | ||
| XR_932841.3:n.1832G>A | ||
| XR_932842.2:n.1832G>A | ||
| XR_932846.3:n.1834G>A | ||
| XR_932847.3:n.1834G>A | ||
| NM_001286403.2:c.860-1973G>A | NP_001273332.1:n.860-1973G>A | |
| NR_104444.2:n.1135+2198G>A | ||
| NM_000246.4:c.1518G>A MANE Select | NP_000237.2:p.Ala506= | |
| NM_001379330.1:c.1374G>A | NP_001366259.1:p.Ala458= | |
| NM_001379331.1:c.1371G>A | NP_001366260.1:p.Ala457= | |
| NM_001379332.1:c.1521G>A | NP_001366261.1:p.Ala507= | |
| NM_001379333.1:c.1518G>A | NP_001366262.1:p.Ala506= | |
| NM_001379334.1:c.1449G>A | NP_001366263.1:p.Ala483= |