LDH info

Canonical Allele Identifier: CA10576160
Gene: SEMA3C HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 226022
ClinVar RCV Id: RCV000211136
dbSNP Id: rs7779029

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.80902796T>C , CM000669.2:g.80902796T>C GRCh38
NC_000007.13:g.80532112T>C , CM000669.1:g.80532112T>C GRCh37
NC_000007.12:g.80370048T>C NCBI36
NG_054744.1:g.24584A>G

Transcript Alleles

HGVS Amino-acid change
NM_006379.3:c.103+13883A>G VV NP_006370.1:p.=
XM_005250113.1:c.-72+3033A>G XP_005250170.1:p.=
NM_001350120.1:c.157+13883A>G VV NP_001337049.1:p.=
NM_001350121.1:c.-72+3033A>G VV NP_001337050.1:p.=
NM_006379.4:c.103+13883A>G VV NP_006370.1:p.=
NM_006379.5:c.103+13883A>G VV MANE Preferred NP_006370.1:p.=
NM_001350120.2:c.157+13883A>G VV NP_001337049.1:p.=
NM_001350121.2:c.-72+3033A>G VV NP_001337050.1:p.=
ENST00000265361.7:c.103+13883A>G ENSP00000265361.3:p.=
ENST00000411788.5:c.191+3033A>G ENSP00000395398.1:p.=
ENST00000419255.6:c.103+13883A>G ENSP00000411193.2:p.=
ENST00000427167.5:c.191+3033A>G ENSP00000399891.1:p.=
ENST00000458729.5:c.103+13883A>G ENSP00000393825.1:p.=
ENST00000487621.5:n.496+13883A>G