Canonical Allele Identifier: CA769999841

Gene:

Linked Data

• dbSNP Id: rs1161894443
• MyVariant Identifiers: chr2:g.52949290A>T (hg19) ; chr2:g.52722152A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.52722152A>T , CM000664.2:g.52722152A>T	GRCh38
NC_000002.11:g.52949290A>T , CM000664.1:g.52949290A>T	GRCh37
NC_000002.10:g.52802794A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_002959384.1:n.1105T>A