Canonical Allele Identifier: CA2197256049
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.94775397C= , CM000677.2:g.94775397C= GRCh38
NC_000015.9:g.95318626C= , CM000677.1:g.95318626C= GRCh37
NC_000015.8:g.93119630C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_932644.1:n.369-9380G=
XR_932644.2:n.369-9380G=