Canonical Allele Identifier: CA709925341
Gene:

Linked Data

dbSNP Id: rs1300447310

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.92307377A>C , CM000676.2:g.92307377A>C GRCh38
NC_000014.8:g.92773721A>C , CM000676.1:g.92773721A>C GRCh37
NC_000014.7:g.91843474A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944153.1:n.131+2833A>C