Linked Data
dbSNP Id:
rs1172145949
gnomAD v2:
7-150883572-A-G
gnomAD v3:
7-151186485-A-G
gnomAD v4:
7-151186485-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.151186485A>G , CM000669.2:g.151186485A>G | GRCh38 |
| NC_000007.13:g.150883572A>G , CM000669.1:g.150883572A>G | GRCh37 |
| NC_000007.12:g.150514505A>G | NCBI36 |
| NG_017016.1:g.6348T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000420175.3:c.491T>C MANE Select | ENSP00000391137.2:p.Val164Ala | |
| ENST00000275838.5:c.491T>C | ENSP00000275838.1:p.Val164Ala | |
| ENST00000377867.7:c.446T>C | ENSP00000367098.3:p.Val149Ala | |
| ENST00000420175.2:c.491T>C | ENSP00000391137.2:p.Val164Ala | |
| NM_001142459.1:c.491T>C | NP_001135931.2:p.Val164Ala | |
| NM_001142460.1:c.491T>C | NP_001135932.2:p.Val164Ala | |
| NM_080871.3:c.446T>C | NP_543147.2:p.Val149Ala | |
| XM_005249949.3:c.626T>C | XP_005250006.1:p.Val209Ala | |
| NM_001142459.2:c.491T>C MANE Select | NP_001135931.2:p.Val164Ala | |
| NM_080871.4:c.446T>C | NP_543147.2:p.Val149Ala |