Canonical Allele Identifier: CA1931617873
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.100101704C= , CM000672.2:g.100101704C= GRCh38
NC_000010.10:g.101861461C= , CM000672.1:g.101861461C= GRCh37
NC_000010.9:g.101851451C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_946245.1:n.185+5467C=