Linked Data
ClinVar Variation Id:
1780660
dbSNP Id:
rs373654559
ExAC:
2:44104758 G / A
gnomAD v2:
2-44104758-G-A
gnomAD v3:
2-43877619-G-A
gnomAD v4:
2-43877619-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.43877619G>A , CM000664.2:g.43877619G>A | GRCh38 |
| NC_000002.11:g.44104758G>A , CM000664.1:g.44104758G>A | GRCh37 |
| NC_000002.10:g.43958262G>A | NCBI36 |
| NG_008884.1:g.43656G>A | |
| NG_008884.2:g.50678G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000272286.4:c.1815G>A MANE Select | ENSP00000272286.2:p.Lys605= | |
| ENST00000272286.2:c.1815G>A | ENSP00000272286.2:p.Lys605= | |
| NM_022437.2:c.1815G>A | NP_071882.1:p.Lys605= | |
| XM_005264483.2:c.1812G>A | XP_005264540.1:p.Lys604= | |
| XM_011533029.1:c.1827G>A | XP_011531331.1:p.Lys609= | |
| XM_011533030.1:c.1824G>A | XP_011531332.1:p.Lys608= | |
| XM_011533031.1:c.1599G>A | XP_011531333.1:p.Lys533= | |
| XR_939707.1:n.2317G>A | ||
| NM_001357321.1:c.1812G>A | NP_001344250.1:p.Lys604= | |
| XM_011533029.2:c.1827G>A | XP_011531331.1:p.Lys609= | |
| XM_011533030.2:c.1824G>A | XP_011531332.1:p.Lys608= | |
| XR_001738891.1:n.2331G>A | ||
| XR_939707.2:n.2331G>A | ||
| NM_022437.3:c.1815G>A MANE Select | NP_071882.1:p.Lys605= | |
| NM_001357321.2:c.1812G>A | NP_001344250.1:p.Lys604= |