Linked Data
ClinVar Variation Id:
2889144
ClinVar RCV Id:
RCV003717641
dbSNP Id:
rs763255801
ExAC:
3:128780690 G / A
gnomAD v2:
3-128780690-G-A
gnomAD v3:
3-129061847-G-A
gnomAD v4:
3-129061847-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.129061847G>A , CM000665.2:g.129061847G>A | GRCh38 |
| NC_000003.11:g.128780690G>A , CM000665.1:g.128780690G>A | GRCh37 |
| NC_000003.10:g.130263380G>A | NCBI36 |
| NG_008715.1:g.6046G>A , LRG_477:g.6046G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307395.5:c.108G>A MANE Select | ENSP00000303942.4:p.Val36= | |
| ENST00000307395.4:c.108G>A | ENSP00000303942.4:p.Val36= | |
| NM_000174.4:c.108G>A , LRG_477t1:c.108G>A | NP_000165.1:p.Val36= | |
| XM_005247374.3:c.108G>A | XP_005247431.1:p.Val36= | |
| XM_011512701.1:c.108G>A | XP_011511003.1:p.Val36= | |
| XM_011512702.1:c.108G>A | XP_011511004.1:p.Val36= | |
| NM_000174.5:c.108G>A MANE Select | NP_000165.1:p.Val36= |