Canonical Allele Identifier: CA2485026928
Gene:

Linked Data

dbSNP Id: rs1703723654

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.211379625C>T , CM000663.2:g.211379625C>T GRCh38
NC_000001.10:g.211552967C>T , CM000663.1:g.211552967C>T GRCh37
NC_000001.9:g.209619590C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001738446.1:n.292-2509G>A