Canonical Allele Identifier: CA856574067
Gene:

Linked Data

dbSNP Id: rs1201455000

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.88981268G>A , CM000670.2:g.88981268G>A GRCh38
NC_000008.10:g.89993497G>A , CM000670.1:g.89993497G>A GRCh37
NC_000008.9:g.90062613G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_002956667.1:n.179-99207C>T