Canonical Allele Identifier: CA2197256013
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.94775288T= , CM000677.2:g.94775288T= GRCh38
NC_000015.9:g.95318517T= , CM000677.1:g.95318517T= GRCh37
NC_000015.8:g.93119521T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_932644.1:n.369-9271A=
XR_932644.2:n.369-9271A=