Canonical Allele Identifier:
CA1657688879
Gene:
Linked Data
dbSNP Id:
rs1776571028
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.117450202C>A , CM000668.2:g.117450202C>A | GRCh38 |
| NC_000006.11:g.117771365C>A , CM000668.1:g.117771365C>A | GRCh37 |
| NC_000006.10:g.117878058C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000467125.1:c.547+116652G>T | ENSP00000487717.1:n.547+116652G>T |