Canonical Allele Identifier: CA1800980002
Gene:

Linked Data

dbSNP Id: rs1808587112

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.88981283G>T , CM000670.2:g.88981283G>T GRCh38
NC_000008.10:g.89993512G>T , CM000670.1:g.89993512G>T GRCh37
NC_000008.9:g.90062628G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_002956667.1:n.179-99222C>A