Canonical Allele Identifier: CA2824549877
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8606165A>G , CM000686.2:g.8606165A>G GRCh38
NC_000024.9:g.8474206A>G , CM000686.1:g.8474206A>G GRCh37
NC_000024.8:g.8534206A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000624507.1:c.53-1134T>C ENSP00000485522.1:n.53-1134T>C
ENST00000624593.1:c.92+16687T>C ENSP00000485106.1:n.92+16687T>C