Canonical Allele Identifier: CA50327959
Gene:

Linked Data

dbSNP Id: rs968953775

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.74711956G>C , CM000664.2:g.74711956G>C GRCh38
NC_000002.11:g.74939083G>C , CM000664.1:g.74939083G>C GRCh37
NC_000002.10:g.74792591G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427047.4:n.269G>C