Canonical Allele Identifier: CA59107039

Gene:

Linked Data

• dbSNP Id: rs913671636
• gnomAD v2: 2-156726690-A-G
• gnomAD v3: 2-155870178-A-G
• gnomAD v4: 2-155870178-A-G
• MyVariant Identifiers: chr2:g.156726690A>G (hg19) ; chr2:g.155870178A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.155870178A>G , CM000664.2:g.155870178A>G	GRCh38
NC_000002.11:g.156726690A>G , CM000664.1:g.156726690A>G	GRCh37
NC_000002.10:g.156434936A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923501.1:n.320-2991T>C
XR_001739749.1:n.331-29194T>C
XR_001739750.1:n.331-29194T>C
XR_001739751.1:n.331-29194T>C
XR_923501.2:n.331-2991T>C