Canonical Allele Identifier: CA2470009402
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8746139T= , CM000686.2:g.8746139T= GRCh38
NC_000024.9:g.8614180T= , CM000686.1:g.8614180T= GRCh37
NC_000024.8:g.8674180T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000624593.1:c.-57+2577A= ENSP00000485106.1:n.-57+2577A=