Canonical Allele Identifier: CA2805109089
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.87152204A>G , CM000677.2:g.87152204A>G GRCh38
NC_000015.9:g.87695435A>G , CM000677.1:g.87695435A>G GRCh37
NC_000015.8:g.85496439A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932582.1:n.167-26023A>G
XR_932582.2:n.167-26023A>G