Linked Data
dbSNP Id:
rs1776778545
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.155427933C>T , CM000668.2:g.155427933C>T | GRCh38 |
| NC_000006.11:g.155749067C>T , CM000668.1:g.155749067C>T | GRCh37 |
| NC_000006.10:g.155790759C>T | NCBI36 |
| NG_011995.1:g.32971G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000159060.3:c.1145+861G>A MANE Select | ENSP00000159060.2:n.1145+861G>A | |
| ENST00000159060.2:c.1145+861G>A | ENSP00000159060.2:n.1145+861G>A | |
| NM_015718.2:c.1145+861G>A | NP_056533.1:n.1145+861G>A | |
| NM_015718.3:c.1145+861G>A MANE Select | NP_056533.1:n.1145+861G>A |