Canonical Allele Identifier: CA759294386

Gene:

Linked Data

• dbSNP Id: rs1365830134
• gnomAD v3: 2-155870508-T-A
• gnomAD v4: 2-155870508-T-A
• MyVariant Identifiers: chr2:g.156727020T>A (hg19) ; chr2:g.155870508T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.155870508T>A , CM000664.2:g.155870508T>A	GRCh38
NC_000002.11:g.156727020T>A , CM000664.1:g.156727020T>A	GRCh37
NC_000002.10:g.156435266T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923501.1:n.320-3321A>T
XR_001739749.1:n.331-29524A>T
XR_001739750.1:n.331-29524A>T
XR_001739751.1:n.331-29524A>T
XR_923501.2:n.331-3321A>T