Canonical Allele Identifier: CA1905920022
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43318662C= , CM000672.2:g.43318662C= GRCh38
NC_000010.10:g.43814110C= , CM000672.1:g.43814110C= GRCh37
NC_000010.9:g.43134116C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945902.1:n.108+67C=
XR_945902.2:n.198+67C=