MyVariant.info:
GRCh37
chr3:g.186650790A>T
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.186933001A>T , CM000665.2:g.186933001A>T | GRCh38 |
| NC_000003.11:g.186650790A>T , CM000665.1:g.186650790A>T | GRCh37 |
| NC_000003.10:g.188133484A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000169298.8:c.-325+2167A>T MANE Select | ENSP00000169298.3:n.-325+2167A>T | |
| ENST00000676786.1:n.510+2167A>T | ||
| ENST00000677292.1:c.-489+2167A>T | ENSP00000503457.1:n.-489+2167A>T | |
| ENST00000169298.7:c.-325+2167A>T | ENSP00000169298.3:n.-325+2167A>T | |
| ENST00000417392.5:c.-325+1607A>T | ENSP00000407631.1:n.-325+1607A>T | |
| ENST00000427315.5:c.-87+2167A>T | ENSP00000412821.1:n.-87+2167A>T | |
| ENST00000430309.5:c.-325+1863A>T | ENSP00000399525.1:n.-325+1863A>T | |
| ENST00000455441.5:c.-229+2167A>T | ENSP00000397273.1:n.-229+2167A>T | |
| ENST00000457772.6:c.-361+2167A>T | ENSP00000412221.2:n.-361+2167A>T | |
| ENST00000458216.5:c.-375+2167A>T | ENSP00000400547.1:n.-375+2167A>T | |
| ENST00000463542.1:n.333+2167A>T | ||
| ENST00000468614.1:n.62+2167A>T | ||
| ENST00000487031.5:n.309+2167A>T | ||
| NM_173216.2:c.-325+2167A>T MANE Select | NP_775323.1:n.-325+2167A>T | |
| NM_173217.2:c.-361+2167A>T | NP_775324.1:n.-361+2167A>T | |
| XM_005247717.2:c.-451+2167A>T | XP_005247774.1:n.-451+2167A>T | |
| XM_006713734.1:c.-580+2167A>T | XP_006713797.1:n.-580+2167A>T | |
| XM_011513085.1:c.-405+2167A>T | XP_011511387.1:n.-405+2167A>T | |
| XR_924163.1:n.350+2167A>T |