Canonical Allele Identifier: CA2223789362
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.55655454A= , CM000678.2:g.55655454A= GRCh38
NC_000016.9:g.55689366A= , CM000678.1:g.55689366A= GRCh37
NC_000016.8:g.54246867A= NCBI36
NG_016969.1:g.4825A=

Transcript Alleles

HGVS Amino-acid change
XR_933603.1:n.54+145T=