Canonical Allele Identifier: CA1012513250
Gene:

Linked Data

dbSNP Id: rs1659289749

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220491648C>T , CM000663.2:g.220491648C>T GRCh38
NC_000001.10:g.220664990C>T , CM000663.1:g.220664990C>T GRCh37
NC_000001.9:g.218731613C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922615.1:n.256-586C>T
XR_001737822.1:n.557-586C>T