Canonical Allele Identifier: CA732182727
Gene:

Linked Data

dbSNP Id: rs1303569863

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.224887089C>G , CM000663.2:g.224887089C>G GRCh38
NC_000001.10:g.225074791C>G , CM000663.1:g.225074791C>G GRCh37
NC_000001.9:g.223141414C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949207.1:n.66-2308G>C
XR_949207.2:n.63-2308G>C