Canonical Allele Identifier: CA1149683777
Gene:

Linked Data

dbSNP Id: rs1644376504

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2567428G>A , CM000663.2:g.2567428G>A GRCh38
NC_000001.10:g.2498867G>A , CM000663.1:g.2498867G>A GRCh37
NC_000001.9:g.2475551C>T NCBI36
NG_047096.1:g.16064G>A

Transcript Alleles

HGVS Amino-acid change
NR_121638.1:n.71+823G>A