LDH info

Canonical Allele Identifier: CA2944680
Gene: UGT2B7 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs28365062

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.69098553A>G , CM000666.2:g.69098553A>G GRCh38
NC_000004.11:g.69964271A>G , CM000666.1:g.69964271A>G GRCh37
NC_000004.10:g.69998860A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001074.2:c.735A>G VV NP_001065.2:p.Thr245=
XM_005265702.2:c.-13A>G XP_005265759.1:p.=
XM_011532229.1:c.735A>G XP_011530531.1:p.Thr245=
XM_011532230.1:c.735A>G XP_011530532.1:p.Thr245=
XM_011532231.1:c.-13A>G XP_011530533.1:p.=
NM_001074.3:c.735A>G VV NP_001065.2:p.Thr245=
NM_001330719.1:c.735A>G VV NP_001317648.1:p.Thr245=
NM_001349568.1:c.-13A>G VV NP_001336497.1:p.=
XM_011532229.2:c.735A>G XP_011530531.1:p.Thr245=
NM_001074.4:c.735A>G VV MANE Preferred NP_001065.2:p.Thr245=
ENST00000305231.11:c.735A>G ENSP00000304811.7:p.Thr245=
ENST00000502942.5:c.-13A>G ENSP00000426206.1:p.=
ENST00000508661.5:c.735A>G ENSP00000427659.1:p.Thr245=
ENST00000509763.1:n.273A>G
ENST00000615638.4:c.*106-93800T>C ENSP00000477842.1:p.=
ENST00000620779.4:c.*380-93800T>C ENSP00000478182.1:p.=
ENST00000622664.1:c.735A>G ENSP00000483172.1:p.Thr245=