LDH info

Canonical Allele Identifier: CA13669591
Gene: IFNG HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2430561

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68158742T>A , CM000674.2:g.68158742T>A GRCh38
NC_000012.11:g.68552522T>A , CM000674.1:g.68552522T>A GRCh37
NC_000012.10:g.66838789T>A NCBI36
NG_015840.1:g.6000A>T

Transcript Alleles

HGVS Amino-acid change
NM_000619.2:c.115-483A>T VV NP_000610.2:p.=
NM_000619.3:c.115-483A>T VV MANE Preferred NP_000610.2:p.=
ENST00000229135.3:c.115-483A>T ENSP00000229135.3:p.=