Canonical Allele Identifier: CA14112099
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.96104564T>A , CM000677.2:g.96104564T>A GRCh38
NC_000015.9:g.96647793T>A , CM000677.1:g.96647793T>A GRCh37
NC_000015.8:g.94448797T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932658.1:n.314-406A>T
NR_158193.1:n.1087-406A>T
XR_001751686.2:n.138-406A>T
XR_002957737.1:n.450+113680T>A