Canonical Allele Identifier: CA2469997964
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8556111G= , CM000686.2:g.8556111G= GRCh38
NC_000024.9:g.8424152G= , CM000686.1:g.8424152G= GRCh37
NC_000024.8:g.8484152G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000624593.1:c.*23-6316C= ENSP00000485106.1:n.*23-6316C=