Canonical Allele Identifier: CA2223789369
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.55655464A= , CM000678.2:g.55655464A= GRCh38
NC_000016.9:g.55689376A= , CM000678.1:g.55689376A= GRCh37
NC_000016.8:g.54246877A= NCBI36
NG_016969.1:g.4835A=

Transcript Alleles

HGVS Amino-acid Change
XR_933603.1:n.54+135T=