Canonical Allele Identifier: CA2470006513
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8690928A= , CM000686.2:g.8690928A= GRCh38
NC_000024.9:g.8558969A= , CM000686.1:g.8558969A= GRCh37
NC_000024.8:g.8618969A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000624593.1:c.-56-32238T= ENSP00000485106.1:n.-56-32238T=