Canonical Allele Identifier: CA1800979873
Gene:

Linked Data

dbSNP Id: rs1808585891

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.88981206C>A , CM000670.2:g.88981206C>A GRCh38
NC_000008.10:g.89993435C>A , CM000670.1:g.89993435C>A GRCh37
NC_000008.9:g.90062551C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_002956667.1:n.179-99145G>T