Linked Data
dbSNP Id:
rs554876233
ExAC:
14:91700787 G / A
gnomAD v2:
14-91700787-G-A
gnomAD v3:
14-91234443-G-A
gnomAD v4:
14-91234443-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.91234443G>A , CM000676.2:g.91234443G>A | GRCh38 |
| NC_000014.8:g.91700787G>A , CM000676.1:g.91700787G>A | GRCh37 |
| NC_000014.7:g.90770540G>A | NCBI36 |
| NG_052988.1:g.24438C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650645.1:c.608C>T MANE Select | ENSP00000498702.1:p.Ala203Val | |
| ENST00000529102.1:c.608C>T | ENSP00000432740.1:p.Ala203Val | |
| ENST00000531499.2:c.608C>T | ENSP00000434045.2:p.Ala203Val | |
| ENST00000535815.5:c.608C>T | ENSP00000440797.1:p.Ala203Val | |
| NM_001177676.1:c.608C>T | NP_001171147.1:p.Ala203Val | |
| NM_003485.3:c.608C>T | NP_003476.3:p.Ala203Val | |
| XM_005268110.3:c.638C>T | XP_005268167.1:p.Ala213Val | |
| XM_005268111.2:c.638C>T | XP_005268168.1:p.Ala213Val | |
| XM_005268112.2:c.638C>T | XP_005268169.1:p.Ala213Val | |
| XM_006720262.2:c.638C>T | XP_006720325.1:p.Ala213Val | |
| XM_011537196.1:c.638C>T | XP_011535498.1:p.Ala213Val | |
| XM_011537197.1:c.638C>T | XP_011535499.1:p.Ala213Val | |
| XM_011537198.1:c.638C>T | XP_011535500.1:p.Ala213Val | |
| XM_011537199.1:c.638C>T | XP_011535501.1:p.Ala213Val | |
| XM_011537200.1:c.638C>T | XP_011535502.1:p.Ala213Val | |
| NM_001348437.1:c.608C>T | NP_001335366.1:p.Ala203Val | |
| XM_005268110.4:c.638C>T | XP_005268167.1:p.Ala213Val | |
| XM_005268111.3:c.638C>T | XP_005268168.1:p.Ala213Val | |
| XM_005268112.3:c.638C>T | XP_005268169.1:p.Ala213Val | |
| XM_006720262.3:c.638C>T | XP_006720325.1:p.Ala213Val | |
| XM_011537196.2:c.638C>T | XP_011535498.1:p.Ala213Val | |
| XM_011537197.3:c.638C>T | XP_011535499.1:p.Ala213Val | |
| XM_011537198.2:c.638C>T | XP_011535500.1:p.Ala213Val | |
| XM_011537199.2:c.638C>T | XP_011535501.1:p.Ala213Val | |
| NM_001177676.2:c.608C>T MANE Select | NP_001171147.1:p.Ala203Val |