Linked Data
ClinVar Variation Id:
407213
dbSNP Id:
rs201939338
ExAC:
5:13794112 G / A
gnomAD v2:
5-13794112-G-A
gnomAD v3:
5-13794003-G-A
gnomAD v4:
5-13794003-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.13794003G>A , CM000667.2:g.13794003G>A | GRCh38 |
| NC_000005.9:g.13794112G>A , CM000667.1:g.13794112G>A | GRCh37 |
| NC_000005.8:g.13847112G>A | NCBI36 |
| NG_013081.1:g.155478C>T | |
| NG_013081.2:g.155478C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265104.5:c.7943C>T MANE Select | ENSP00000265104.4:p.Ala2648Val | |
| ENST00000681290.1:c.7898C>T | ENSP00000505288.1:p.Ala2633Val | |
| ENST00000265104.4:c.7943C>T | ENSP00000265104.4:p.Ala2648Val | |
| NM_001369.2:c.7943C>T | NP_001360.1:p.Ala2648Val | |
| XM_005248262.2:c.7898C>T | XP_005248319.1:p.Ala2633Val | |
| XM_011513990.1:c.7943C>T | XP_011512292.1:p.Ala2648Val | |
| XR_925598.1:n.8150C>T | ||
| XM_005248262.3:c.8051C>T | XP_005248319.2:p.Ala2684Val | |
| XM_017009177.1:c.8051C>T | XP_016864666.1:p.Ala2684Val | |
| XM_017009178.1:c.6956C>T | XP_016864667.1:p.Ala2319Val | |
| XM_017009179.2:c.6956C>T | XP_016864668.1:p.Ala2319Val | |
| XM_017009180.1:c.8051C>T | XP_016864669.1:p.Ala2684Val | |
| XM_017009181.1:c.8051C>T | XP_016864670.1:p.Ala2684Val | |
| XM_017009182.1:c.8051C>T | XP_016864671.1:p.Ala2684Val | |
| XM_017009183.1:c.8051C>T | XP_016864672.1:p.Ala2684Val | |
| XM_017009184.1:c.8051C>T | XP_016864673.1:p.Ala2684Val | |
| XM_017009185.1:c.3140C>T | XP_016864674.1:p.Ala1047Val | |
| XM_017009186.1:c.2693C>T | XP_016864675.1:p.Ala898Val | |
| XM_017009187.1:c.*46C>T | XP_016864676.1:n.*46C>T | |
| XM_017009188.1:c.2030C>T | XP_016864677.1:p.Ala677Val | |
| XM_024454388.1:c.6956C>T | XP_024310156.1:p.Ala2319Val | |
| XM_024454389.1:c.6545C>T | XP_024310157.1:p.Ala2182Val | |
| XR_001742034.1:n.8068C>T | ||
| XR_001742035.1:n.8068C>T | ||
| NM_001369.3:c.7943C>T MANE Select | NP_001360.1:p.Ala2648Val |