Canonical Allele Identifier: CA487780632
Gene:

Linked Data

dbSNP Id: rs1182713647

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.92307267A>G , CM000676.2:g.92307267A>G GRCh38
NC_000014.8:g.92773611A>G , CM000676.1:g.92773611A>G GRCh37
NC_000014.7:g.91843364A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_944153.1:n.131+2723A>G