Canonical Allele Identifier: CA265579794
Gene:

Linked Data

dbSNP Id: rs1007498012

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.92307384G>C , CM000676.2:g.92307384G>C GRCh38
NC_000014.8:g.92773728G>C , CM000676.1:g.92773728G>C GRCh37
NC_000014.7:g.91843481G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944153.1:n.131+2840G>C