Canonical Allele Identifier: CA669472919
Gene:

Linked Data

dbSNP Id: rs1348023124

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8697676G>C , CM000672.2:g.8697676G>C GRCh38
NC_000010.10:g.8739639G>C , CM000672.1:g.8739639G>C GRCh37
NC_000010.9:g.8779645G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930641.1:n.33-27875C>G