Canonical Allele Identifier: CA1905920011
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43318630C= , CM000672.2:g.43318630C= GRCh38
NC_000010.10:g.43814078C= , CM000672.1:g.43814078C= GRCh37
NC_000010.9:g.43134084C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945902.1:n.108+35C=
XR_945902.2:n.198+35C=