Linked Data
dbSNP Id:
rs1015619587
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.29534052A>T , CM000679.2:g.29534052A>T | GRCh38 |
| NC_000017.10:g.27861070A>T , CM000679.1:g.27861070A>T | GRCh37 |
| NC_000017.9:g.24885196A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000261716.8:c.2362-66A>T MANE Select | ENSP00000261716.3:n.2362-66A>T | |
| ENST00000261716.7:c.2362-66A>T | ENSP00000261716.3:n.2362-66A>T | |
| ENST00000536202.1:c.1918-66A>T | ENSP00000438819.1:n.1918-66A>T | |
| NM_020791.2:c.2362-66A>T | NP_065842.1:n.2362-66A>T | |
| NM_025142.1:c.1918-66A>T | NP_079418.1:n.1918-66A>T | |
| XM_011525060.1:c.2362-66A>T | XP_011523362.1:n.2362-66A>T | |
| XM_011525060.2:c.2362-66A>T | XP_011523362.1:n.2362-66A>T | |
| NM_020791.4:c.2362-66A>T MANE Select | NP_065842.1:n.2362-66A>T |