Canonical Allele Identifier: CA16339998
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.78488803A>G , CM000670.2:g.78488803A>G GRCh38
NC_000008.10:g.79401038A>G , CM000670.1:g.79401038A>G GRCh37
NC_000008.9:g.79563593A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929074.1:n.1089-57855T>C
XR_001745972.1:n.1077-57855T>C