Canonical Allele Identifier: CA1800979975
Gene:

Linked Data

dbSNP Id: rs1808586725

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.88981260G>A , CM000670.2:g.88981260G>A GRCh38
NC_000008.10:g.89993489G>A , CM000670.1:g.89993489G>A GRCh37
NC_000008.9:g.90062605G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_002956667.1:n.179-99199C>T