Canonical Allele Identifier: CA937524919
Gene:

Linked Data

dbSNP Id: rs1856778039

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45506520A>G , CM000673.2:g.45506520A>G GRCh38
NC_000011.9:g.45528070A>G , CM000673.1:g.45528070A>G GRCh37
NC_000011.8:g.45484646A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001748204.2:n.909-16749T>C
XR_931245.3:n.566-16749T>C