Linked Data
dbSNP Id:
rs1472889632
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.40644323C>A , CM000675.2:g.40644323C>A | GRCh38 |
| NC_000013.10:g.41218460C>A , CM000675.1:g.41218460C>A | GRCh37 |
| NC_000013.9:g.40116460C>A | NCBI36 |
| NG_023244.1:g.27275G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379561.6:c.630+21260G>T MANE Select | ENSP00000368880.4:n.630+21260G>T | |
| ENST00000655267.1:n.333+21260G>T | ||
| ENST00000660760.1:n.296-11075G>T | ||
| ENST00000379561.5:c.630+21260G>T | ENSP00000368880.4:n.630+21260G>T | |
| NM_002015.3:c.630+21260G>T | NP_002006.2:n.630+21260G>T | |
| XR_941536.1:n.1226+1016G>T | ||
| NM_002015.4:c.630+21260G>T MANE Select | NP_002006.2:n.630+21260G>T |