Canonical Allele Identifier: CA47693328

Gene:

Linked Data

• dbSNP Id: rs987573924
• MyVariant Identifiers: chr2:g.52949530A>G (hg19) ; chr2:g.52722392A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.52722392A>G , CM000664.2:g.52722392A>G	GRCh38
NC_000002.11:g.52949530A>G , CM000664.1:g.52949530A>G	GRCh37
NC_000002.10:g.52803034A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_002959384.1:n.865T>C