Canonical Allele Identifier: CA1038177623

Gene:

Linked Data

• dbSNP Id: rs1683152950
• gnomAD v3: 2-155870727-A-C
• gnomAD v4: 2-155870727-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.155870727A>C , CM000664.2:g.155870727A>C	GRCh38
NC_000002.11:g.156727239A>C , CM000664.1:g.156727239A>C	GRCh37
NC_000002.10:g.156435485A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923501.1:n.320-3540T>G
XR_001739749.1:n.331-29743T>G
XR_001739750.1:n.331-29743T>G
XR_001739751.1:n.331-29743T>G
XR_923501.2:n.331-3540T>G