LDH info

Canonical Allele Identifier: CA1407165
Gene: MIA3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs17465637

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.222650187A>C , CM000663.2:g.222650187A>C GRCh38
NC_000001.10:g.222823529A>C , CM000663.1:g.222823529A>C GRCh37
NC_000001.9:g.220890152A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001300867.1:c.266-105A>C VV NP_001287796.1:p.=
NM_198551.3:c.3632-105A>C VV NP_940953.2:p.=
XM_005273121.3:c.3632-105A>C XP_005273178.1:p.=
XM_006711304.2:c.3632-105A>C XP_006711367.1:p.=
XM_011509513.1:c.3632-105A>C XP_011507815.1:p.=
NM_001324062.1:c.3632-105A>C VV NP_001310991.1:p.=
NM_001324063.1:c.3632-105A>C VV NP_001310992.1:p.=
NM_001324064.1:c.3140-105A>C VV NP_001310993.1:p.=
NM_001324065.1:c.266-105A>C VV NP_001310994.1:p.=
XM_006711304.4:c.3632-105A>C XP_006711367.3:p.=
XM_011509513.3:c.3632-105A>C XP_011507815.3:p.=
XM_017001243.2:c.3140-105A>C XP_016856732.1:p.=
NM_198551.4:c.3632-105A>C VV MANE Preferred NP_940953.2:p.=
ENST00000340535.11:c.266-105A>C ENSP00000345866.7:p.=
ENST00000344507.1:c.1475-15412A>C ENSP00000341348.1:p.=
ENST00000344922.9:c.3632-105A>C ENSP00000340900.5:p.=
ENST00000354906.7:n.2379-105A>C
ENST00000467190.1:n.530-105A>C
ENST00000495210.1:n.326-105A>C