Canonical Allele Identifier: CA181599890
Gene:

Linked Data

dbSNP Id: rs970503379

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.88981306C>T , CM000670.2:g.88981306C>T GRCh38
NC_000008.10:g.89993535C>T , CM000670.1:g.89993535C>T GRCh37
NC_000008.9:g.90062651C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_002956667.1:n.179-99245G>A