Canonical Allele Identifier: CA2051430491
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.84952199T= , CM000674.2:g.84952199T= GRCh38
NC_000012.11:g.85345978T= , CM000674.1:g.85345978T= GRCh37
NC_000012.10:g.83870109T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945152.1:n.316+30885T=
XR_945153.1:n.301+13735T=
XR_945154.1:n.175-36743T=
XR_945155.1:n.330+30885T=
XR_945152.2:n.316+30885T=
XR_945154.2:n.175-36743T=
XR_945155.2:n.888+30885T=