Canonical Allele Identifier: CA658593969
Gene:

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8556190G>A , CM000686.2:g.8556190G>A GRCh38
NC_000024.9:g.8424231G>A , CM000686.1:g.8424231G>A GRCh37
NC_000024.8:g.8484231G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000624593.1:c.*23-6395C>T ENSP00000485106.1:n.*23-6395C>T