Canonical Allele Identifier: CA2562072376
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8556052T>C , CM000686.2:g.8556052T>C GRCh38
NC_000024.9:g.8424093T>C , CM000686.1:g.8424093T>C GRCh37
NC_000024.8:g.8484093T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000624593.1:c.*23-6257A>G ENSP00000485106.1:n.*23-6257A>G