Canonical Allele Identifier: CA16373882
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.121565769T>G , CM000671.2:g.121565769T>G GRCh38
NC_000009.11:g.124328048T>G , CM000671.1:g.124328048T>G GRCh37
NC_000009.10:g.123367869T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746560.1:n.2055+1082A>C