Canonical Allele Identifier: CA537204386

Gene:

Linked Data

• dbSNP Id: rs1323641348
• gnomAD v2: 2-156726974-G-A
• gnomAD v3: 2-155870462-G-A
• gnomAD v4: 2-155870462-G-A
• MyVariant Identifiers: chr2:g.156726974G>A (hg19) ; chr2:g.155870462G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.155870462G>A , CM000664.2:g.155870462G>A	GRCh38
NC_000002.11:g.156726974G>A , CM000664.1:g.156726974G>A	GRCh37
NC_000002.10:g.156435220G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923501.1:n.320-3275C>T
XR_001739749.1:n.331-29478C>T
XR_001739750.1:n.331-29478C>T
XR_001739751.1:n.331-29478C>T
XR_923501.2:n.331-3275C>T