Canonical Allele Identifier: CA1266890423
Gene: GNLY HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85693267G= , CM000664.2:g.85693267G= GRCh38
NC_000002.11:g.85920390G= , CM000664.1:g.85920390G= GRCh37
NC_000002.10:g.85773901G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000488945.5:n.48-2053G=