Canonical Allele Identifier: CA2223789372
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.55655473T= , CM000678.2:g.55655473T= GRCh38
NC_000016.9:g.55689385T= , CM000678.1:g.55689385T= GRCh37
NC_000016.8:g.54246886T= NCBI36
NG_016969.1:g.4844T=

Transcript Alleles

HGVS Amino-acid Change
XR_933603.1:n.54+126A=