Canonical Allele Identifier: CA73026652

Gene:

Linked Data

• dbSNP Id: rs949672166
• MyVariant Identifiers: chr3:g.39263207G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39263207G>C , CM000665.2:g.39263207G>C	GRCh38
NC_000003.11:g.39304698G>C , CM000665.1:g.39304698G>C	GRCh37
NC_000003.10:g.39279702G>C	NCBI36
NG_016362.1:g.23529C>G

Transcript Alleles

HGVS	Amino-acid change
XR_001740660.2:n.2724G>C