Linked Data
ClinVar Variation Id:
3081905
ClinVar RCV Id:
RCV004371261
dbSNP Id:
rs770071397
ExAC:
3:123003524 G / A
gnomAD v2:
3-123003524-G-A
gnomAD v3:
3-123284677-G-A
gnomAD v4:
3-123284677-G-A
PubMed:
PMID:28135719
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.123284677G>A , CM000665.2:g.123284677G>A | GRCh38 |
| NC_000003.11:g.123003524G>A , CM000665.1:g.123003524G>A | GRCh37 |
| NC_000003.10:g.124486214G>A | NCBI36 |
| NG_033882.1:g.168869C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000466617.6:c.2394C>T | ENSP00000420082.2:p.Gly798= | |
| ENST00000470367.2:c.2682C>T | ENSP00000514541.1:p.Gly894= | |
| ENST00000483566.2:c.2394C>T | ENSP00000420252.2:p.Gly798= | |
| ENST00000699714.1:c.2394C>T | ENSP00000514539.1:p.Gly798= | |
| ENST00000699715.1:c.2394C>T | ENSP00000514540.1:p.Gly798= | |
| ENST00000699716.1:c.2394C>T | ENSP00000514542.1:p.Gly798= | |
| ENST00000699717.1:n.2120C>T | ||
| ENST00000699718.1:c.3792C>T | ENSP00000514543.1:p.Gly1264= | |
| ENST00000462833.6:c.3717C>T MANE Select | ENSP00000419361.1:p.Gly1239= | |
| ENST00000309879.9:c.2667C>T | ENSP00000308685.5:p.Gly889= | |
| ENST00000462833.5:c.3717C>T | ENSP00000419361.1:p.Gly1239= | |
| ENST00000478092.1:n.487C>T | ||
| ENST00000491190.5:c.2691C>T | ENSP00000418537.1:p.Gly897= | |
| NM_001199642.1:c.2667C>T | NP_001186571.1:p.Gly889= | |
| NM_183357.2:c.3717C>T | NP_899200.1:p.Gly1239= | |
| XM_005247077.2:c.3792C>T | XP_005247134.1:p.Gly1264= | |
| XM_005247078.1:c.2742C>T | XP_005247135.1:p.Gly914= | |
| XM_006713483.1:c.2691C>T | XP_006713546.1:p.Gly897= | |
| XM_006713484.1:c.2469C>T | XP_006713547.1:p.Gly823= | |
| XM_011512359.1:c.2793C>T | XP_011510661.1:p.Gly931= | |
| XM_011512360.1:c.2703C>T | XP_011510662.1:p.Gly901= | |
| XM_011512361.1:c.2469C>T | XP_011510663.1:p.Gly823= | |
| XM_005247077.4:c.3792C>T | XP_005247134.1:p.Gly1264= | |
| XM_011512359.2:c.2793C>T | XP_011510661.1:p.Gly931= | |
| XM_011512360.3:c.2703C>T | XP_011510662.1:p.Gly901= | |
| XM_017005638.1:c.2694C>T | XP_016861127.1:p.Gly898= | |
| XM_017005639.1:c.2694C>T | XP_016861128.1:p.Gly898= | |
| NM_001378259.1:c.3792C>T | NP_001365188.1:p.Gly1264= | |
| NM_183357.3:c.3717C>T MANE Select | NP_899200.1:p.Gly1239= |