Canonical Allele Identifier: CA59107079

Gene:

Linked Data

• dbSNP Id: rs928781323
• gnomAD v2: 2-156727056-A-T
• gnomAD v3: 2-155870544-A-T
• gnomAD v4: 2-155870544-A-T
• MyVariant Identifiers: chr2:g.156727056A>T (hg19) ; chr2:g.155870544A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.155870544A>T , CM000664.2:g.155870544A>T	GRCh38
NC_000002.11:g.156727056A>T , CM000664.1:g.156727056A>T	GRCh37
NC_000002.10:g.156435302A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923501.1:n.320-3357T>A
XR_001739749.1:n.331-29560T>A
XR_001739750.1:n.331-29560T>A
XR_001739751.1:n.331-29560T>A
XR_923501.2:n.331-3357T>A