Canonical Allele Identifier: CA965992692
Gene:

Linked Data

dbSNP Id: rs1884566089

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.92307358A>G , CM000676.2:g.92307358A>G GRCh38
NC_000014.8:g.92773702A>G , CM000676.1:g.92773702A>G GRCh37
NC_000014.7:g.91843455A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944153.1:n.131+2814A>G