Canonical Allele Identifier: CA59107080

Gene:

Linked Data

• dbSNP Id: rs370802064
• gnomAD v3: 2-155870546-G-A
• gnomAD v4: 2-155870546-G-A
• MyVariant Identifiers: chr2:g.156727058G>A (hg19) ; chr2:g.155870546G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.155870546G>A , CM000664.2:g.155870546G>A	GRCh38
NC_000002.11:g.156727058G>A , CM000664.1:g.156727058G>A	GRCh37
NC_000002.10:g.156435304G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923501.1:n.320-3359C>T
XR_001739749.1:n.331-29562C>T
XR_001739750.1:n.331-29562C>T
XR_001739751.1:n.331-29562C>T
XR_923501.2:n.331-3359C>T