LDH info

Canonical Allele Identifier: CA11349876
Gene: OXTR HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs4564970

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8768722G>C , CM000665.2:g.8768722G>C GRCh38
NC_000003.11:g.8810408G>C , CM000665.1:g.8810408G>C GRCh37
NC_000003.10:g.8785408G>C NCBI36
NG_008797.2:g.39913G>C , LRG_329:g.39913G>C

Transcript Alleles

HGVS Amino-acid change
NM_000916.3:c.-238-131C>G VV NP_000907.2:p.=
XM_011533762.1:c.-238-131C>G XP_011532064.1:p.=
XM_011533763.1:c.-238-131C>G XP_011532065.1:p.=
NM_001354653.1:c.-238-131C>G VV NP_001341582.1:p.=
NM_001354654.1:c.-238-131C>G VV NP_001341583.1:p.=
NM_001354655.1:c.-238-131C>G VV NP_001341584.1:p.=
NM_001354656.1:c.-273C>G VV NP_001341585.1:p.=
NM_001354656.2:c.-273C>G VV NP_001341585.1:p.=
NM_000916.4:c.-238-131C>G VV NP_000907.2:p.=
NM_001354653.2:c.-238-131C>G VV NP_001341582.1:p.=
NM_001354654.2:c.-238-131C>G VV NP_001341583.1:p.=
NM_001354655.2:c.-238-131C>G VV NP_001341584.1:p.=
NM_001354656.3:c.-273C>G VV NP_001341585.1:p.=
ENST00000316793.7:c.-238-131C>G ENSP00000324270.2:p.=
ENST00000431493.1:c.-238-131C>G ENSP00000414828.1:p.=
ENST00000472766.1:n.156-8755G>C
ENST00000474615.1:n.384-131C>G