Canonical Allele Identifier: CA926324521
Gene:

Linked Data

dbSNP Id: rs1835464908

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.29075775C>T , CM000672.2:g.29075775C>T GRCh38
NC_000010.10:g.29364704C>T , CM000672.1:g.29364704C>T GRCh37
NC_000010.9:g.29404710C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001747284.1:n.127-3717C>T