Canonical Allele Identifier: CA1038177543

Gene:

Linked Data

• dbSNP Id: rs1683146730
• gnomAD v3: 2-155870545-G-A
• gnomAD v4: 2-155870545-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.155870545G>A , CM000664.2:g.155870545G>A	GRCh38
NC_000002.11:g.156727057G>A , CM000664.1:g.156727057G>A	GRCh37
NC_000002.10:g.156435303G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923501.1:n.320-3358C>T
XR_001739749.1:n.331-29561C>T
XR_001739750.1:n.331-29561C>T
XR_001739751.1:n.331-29561C>T
XR_923501.2:n.331-3358C>T