Canonical Allele Identifier: CA59107102

Gene:

Linked Data

• dbSNP Id: rs367717234
• gnomAD v2: 2-156727189-C-T
• gnomAD v3: 2-155870677-C-T
• gnomAD v4: 2-155870677-C-T
• MyVariant Identifiers: chr2:g.156727189C>T (hg19) ; chr2:g.155870677C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.155870677C>T , CM000664.2:g.155870677C>T	GRCh38
NC_000002.11:g.156727189C>T , CM000664.1:g.156727189C>T	GRCh37
NC_000002.10:g.156435435C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923501.1:n.320-3490G>A
XR_001739749.1:n.331-29693G>A
XR_001739750.1:n.331-29693G>A
XR_001739751.1:n.331-29693G>A
XR_923501.2:n.331-3490G>A