Canonical Allele Identifier: CA287548483
Gene:

Linked Data

dbSNP Id: rs916747574

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8137373C>T , CM000679.2:g.8137373C>T GRCh38
NC_000017.10:g.8040691C>T , CM000679.1:g.8040691C>T GRCh37
NC_000017.9:g.7981416C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934202.1:n.183-1476C>T
XR_934203.1:n.70-2104C>T
XR_934202.2:n.414-1476C>T