Canonical Allele Identifier: CA2469997958
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8556048A= , CM000686.2:g.8556048A= GRCh38
NC_000024.9:g.8424089A= , CM000686.1:g.8424089A= GRCh37
NC_000024.8:g.8484089A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000624593.1:c.*23-6253T= ENSP00000485106.1:n.*23-6253T=