Canonical Allele Identifier: CA856574099
Gene:

Linked Data

dbSNP Id: rs1217466874

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.88981300C>T , CM000670.2:g.88981300C>T GRCh38
NC_000008.10:g.89993529C>T , CM000670.1:g.89993529C>T GRCh37
NC_000008.9:g.90062645C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_002956667.1:n.179-99239G>A