Canonical Allele Identifier: CA337622086
Gene:

Linked Data

dbSNP Id: rs776843538

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8556246A>G , CM000686.2:g.8556246A>G GRCh38
NC_000024.9:g.8424287A>G , CM000686.1:g.8424287A>G GRCh37
NC_000024.8:g.8484287A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000624593.1:c.*23-6451T>C ENSP00000485106.1:n.*23-6451T>C