Canonical Allele Identifier: CA1573962528
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113714823C= , CM000667.2:g.113714823C= GRCh38
NC_000005.9:g.113050520C= , CM000667.1:g.113050520C= GRCh37
NC_000005.8:g.113078419C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001742840.1:n.153-18738C=