LDH info

Canonical Allele Identifier: CA12635034
Gene: HGF HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2286194

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.81726133T>A , CM000669.2:g.81726133T>A GRCh38
NC_000007.13:g.81355449T>A , CM000669.1:g.81355449T>A GRCh37
NC_000007.12:g.81193385T>A NCBI36
NG_016274.1:g.49004A>T
NG_016274.2:g.49004A>T

Transcript Alleles

HGVS Amino-acid change
NM_000601.4:c.1041-116A>T VV NP_000592.3:p.=
NM_001010932.1:c.1026-116A>T VV NP_001010932.1:p.=
XM_006715956.2:c.1041-116A>T XP_006716019.1:p.=
XM_011516115.1:c.1026-116A>T XP_011514417.1:p.=
NM_000601.5:c.1041-116A>T VV NP_000592.3:p.=
NM_001010932.2:c.1026-116A>T VV NP_001010932.1:p.=
XM_011516115.2:c.1026-116A>T XP_011514417.1:p.=
NM_000601.6:c.1041-116A>T VV MANE Preferred NP_000592.3:p.=
ENST00000222390.9:c.1041-116A>T ENSP00000222390.5:p.=
ENST00000457544.6:c.1026-116A>T ENSP00000391238.2:p.=