Canonical Allele Identifier: CA1014751132
Gene:

Linked Data

dbSNP Id: rs1983026561
gnomAD v3: 20-1875469-A-C
gnomAD v4: 20-1875469-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.1875469A>C , CM000682.2:g.1875469A>C GRCh38
NC_000020.10:g.1856115A>C , CM000682.1:g.1856115A>C GRCh37
NC_000020.9:g.1804115A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001754467.1:n.433-7376T>G