Canonical Allele Identifier: CA2197256029
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.94775332G= , CM000677.2:g.94775332G= GRCh38
NC_000015.9:g.95318561G= , CM000677.1:g.95318561G= GRCh37
NC_000015.8:g.93119565G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_932644.1:n.369-9315C=
XR_932644.2:n.369-9315C=