Linked Data
dbSNP Id:
rs770352171
ExAC:
12:129299411 G / A
gnomAD v2:
12-129299411-G-A
gnomAD v3:
12-128814866-G-A
gnomAD v4:
12-128814866-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.128814866G>A , CM000674.2:g.128814866G>A | GRCh38 |
| NC_000012.11:g.129299411G>A , CM000674.1:g.129299411G>A | GRCh37 |
| NC_000012.10:g.127865364G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266771.10:c.751C>T MANE Select | ENSP00000266771.5:p.Pro251Ser | |
| ENST00000266771.9:c.751C>T | ENSP00000266771.5:p.Pro251Ser | |
| ENST00000366292.6:n.1063C>T | ||
| ENST00000376740.8:c.330C>T | ||
| ENST00000376744.8:c.587C>T | ||
| ENST00000539703.1:n.401C>T | ||
| ENST00000614634.1:c.-92C>T | ENSP00000483143.1:n.-92C>T | |
| NM_145648.3:c.751C>T | NP_663623.1:p.Pro251Ser | |
| XM_011537895.1:c.901C>T | XP_011536197.1:p.Pro301Ser | |
| XR_429081.2:n.774C>T | ||
| XR_944494.1:n.924C>T | ||
| XR_944495.1:n.924C>T | ||
| XR_944496.1:n.924C>T | ||
| XR_944497.1:n.924C>T | ||
| XM_017018791.1:c.901C>T | XP_016874280.1:p.Pro301Ser | |
| XM_017018792.1:c.901C>T | XP_016874281.1:p.Pro301Ser | |
| XM_017018793.1:c.751C>T | XP_016874282.1:p.Pro251Ser | |
| XR_002957287.1:n.774C>T | ||
| XR_944496.2:n.924C>T | ||
| NM_145648.4:c.751C>T MANE Select | NP_663623.1:p.Pro251Ser |