Canonical Allele Identifier: CA2223789412
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.55655564C= , CM000678.2:g.55655564C= GRCh38
NC_000016.9:g.55689476C= , CM000678.1:g.55689476C= GRCh37
NC_000016.8:g.54246977C= NCBI36
NG_016969.1:g.4935C=

Transcript Alleles

HGVS Amino-acid change
XR_933603.1:n.54+35G=