Canonical Allele Identifier: CA2713400281
Gene:

Linked Data

dbSNP Id: rs2115164359

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151627148G>A , CM000668.2:g.151627148G>A GRCh38
NC_000006.11:g.151948283G>A , CM000668.1:g.151948283G>A GRCh37
NC_000006.10:g.151989976G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943113.1:n.574G>A
XR_943115.1:n.574G>A