Linked Data
dbSNP Id:
rs534616954
gnomAD v2:
14-91700761-C-T
gnomAD v3:
14-91234417-C-T
gnomAD v4:
14-91234417-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.91234417C>T , CM000676.2:g.91234417C>T | GRCh38 |
| NC_000014.8:g.91700761C>T , CM000676.1:g.91700761C>T | GRCh37 |
| NC_000014.7:g.90770514C>T | NCBI36 |
| NG_052988.1:g.24464G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650645.1:c.634G>A MANE Select | ENSP00000498702.1:p.Val212Met | |
| ENST00000529102.1:c.634G>A | ENSP00000432740.1:p.Val212Met | |
| ENST00000531499.2:c.634G>A | ENSP00000434045.2:p.Val212Met | |
| ENST00000535815.5:c.634G>A | ENSP00000440797.1:p.Val212Met | |
| NM_001177676.1:c.634G>A | NP_001171147.1:p.Val212Met | |
| NM_003485.3:c.634G>A | NP_003476.3:p.Val212Met | |
| XM_005268110.3:c.664G>A | XP_005268167.1:p.Val222Met | |
| XM_005268111.2:c.664G>A | XP_005268168.1:p.Val222Met | |
| XM_005268112.2:c.664G>A | XP_005268169.1:p.Val222Met | |
| XM_006720262.2:c.664G>A | XP_006720325.1:p.Val222Met | |
| XM_011537196.1:c.664G>A | XP_011535498.1:p.Val222Met | |
| XM_011537197.1:c.664G>A | XP_011535499.1:p.Val222Met | |
| XM_011537198.1:c.664G>A | XP_011535500.1:p.Val222Met | |
| XM_011537199.1:c.664G>A | XP_011535501.1:p.Val222Met | |
| XM_011537200.1:c.664G>A | XP_011535502.1:p.Val222Met | |
| NM_001348437.1:c.634G>A | NP_001335366.1:p.Val212Met | |
| XM_005268110.4:c.664G>A | XP_005268167.1:p.Val222Met | |
| XM_005268111.3:c.664G>A | XP_005268168.1:p.Val222Met | |
| XM_005268112.3:c.664G>A | XP_005268169.1:p.Val222Met | |
| XM_006720262.3:c.664G>A | XP_006720325.1:p.Val222Met | |
| XM_011537196.2:c.664G>A | XP_011535498.1:p.Val222Met | |
| XM_011537197.3:c.664G>A | XP_011535499.1:p.Val222Met | |
| XM_011537198.2:c.664G>A | XP_011535500.1:p.Val222Met | |
| XM_011537199.2:c.664G>A | XP_011535501.1:p.Val222Met | |
| NM_001177676.2:c.634G>A MANE Select | NP_001171147.1:p.Val212Met |