Canonical Allele Identifier: CA313629813
Gene:

Linked Data

dbSNP Id: rs189615149

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23661829G>C , CM000682.2:g.23661829G>C GRCh38
NC_000020.10:g.23642466G>C , CM000682.1:g.23642466G>C GRCh37
NC_000020.9:g.23590466G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001754712.1:n.280+179G>C