Canonical Allele Identifier: CA1266890440
Gene: GNLY HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85693303C= , CM000664.2:g.85693303C= GRCh38
NC_000002.11:g.85920426C= , CM000664.1:g.85920426C= GRCh37
NC_000002.10:g.85773937C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000488945.5:n.48-2017C=