Canonical Allele Identifier: CA770000083

Gene:

Linked Data

• dbSNP Id: rs1203564628
• MyVariant Identifiers: chr2:g.52949605T>C (hg19) ; chr2:g.52722467T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.52722467T>C , CM000664.2:g.52722467T>C	GRCh38
NC_000002.11:g.52949605T>C , CM000664.1:g.52949605T>C	GRCh37
NC_000002.10:g.52803109T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_002959384.1:n.790A>G