Canonical Allele Identifier: CA2717760061
Gene:

Linked Data

dbSNP Id: rs1295018540

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.88981311C>T , CM000670.2:g.88981311C>T GRCh38
NC_000008.10:g.89993540C>T , CM000670.1:g.89993540C>T GRCh37
NC_000008.9:g.90062656C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002956667.1:n.179-99250G>A