Canonical Allele Identifier: CA14232783
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.85939422T>C , CM000678.2:g.85939422T>C GRCh38
NC_000016.9:g.85973028T>C , CM000678.1:g.85973028T>C GRCh37
NC_000016.8:g.84530529T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_933852.1:n.466-5994T>C
XR_933853.1:n.466-5994T>C