Canonical Allele Identifier: CA2469997939
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8555976G= , CM000686.2:g.8555976G= GRCh38
NC_000024.9:g.8424017G= , CM000686.1:g.8424017G= GRCh37
NC_000024.8:g.8484017G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000624593.1:c.*23-6181C= ENSP00000485106.1:n.*23-6181C=