Canonical Allele Identifier: CA759294310

Gene:

Linked Data

• dbSNP Id: rs1436919385
• MyVariant Identifiers: chr2:g.156726896C>A (hg19) ; chr2:g.155870384C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.155870384C>A , CM000664.2:g.155870384C>A	GRCh38
NC_000002.11:g.156726896C>A , CM000664.1:g.156726896C>A	GRCh37
NC_000002.10:g.156435142C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923501.1:n.320-3197G>T
XR_001739749.1:n.331-29400G>T
XR_001739750.1:n.331-29400G>T
XR_001739751.1:n.331-29400G>T
XR_923501.2:n.331-3197G>T