Canonical Allele Identifier: CA313629787
Gene:

Linked Data

dbSNP Id: rs530705608

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23661794G>A , CM000682.2:g.23661794G>A GRCh38
NC_000020.10:g.23642431G>A , CM000682.1:g.23642431G>A GRCh37
NC_000020.9:g.23590431G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001754712.1:n.280+144G>A