Canonical Allele Identifier: CA1573933677
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113660965C= , CM000667.2:g.113660965C= GRCh38
NC_000005.9:g.112996662C= , CM000667.1:g.112996662C= GRCh37
NC_000005.8:g.113024561C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001742841.1:n.59+27601C=