Canonical Allele Identifier: CA2550664464
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8556171C>T , CM000686.2:g.8556171C>T GRCh38
NC_000024.9:g.8424212C>T , CM000686.1:g.8424212C>T GRCh37
NC_000024.8:g.8484212C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000624593.1:c.*23-6376G>A ENSP00000485106.1:n.*23-6376G>A