Canonical Allele Identifier: CA1266890375
Gene: GNLY HGNC NCBI

Linked Data

dbSNP Id: rs1678294386
gnomAD v3: 2-85693168-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85693168T>C , CM000664.2:g.85693168T>C GRCh38
NC_000002.11:g.85920291T>C , CM000664.1:g.85920291T>C GRCh37
NC_000002.10:g.85773802T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000488945.5:n.48-2152T>C