Canonical Allele Identifier: CA1266890399
Gene: GNLY HGNC NCBI

Linked Data

dbSNP Id: rs2886767

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85693206T>G , CM000664.2:g.85693206T>G GRCh38
NC_000002.11:g.85920329T>G , CM000664.1:g.85920329T>G GRCh37
NC_000002.10:g.85773840T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000488945.5:n.48-2114T>G