LDH info

Canonical Allele Identifier: CA16118797
Gene: MYO3B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10176755

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.170509379A>G , CM000664.2:g.170509379A>G GRCh38
NC_000002.11:g.171365889A>G , CM000664.1:g.171365889A>G GRCh37
NC_000002.10:g.171074135A>G NCBI36
NG_034020.1:g.336235A>G

Transcript Alleles

HGVS Amino-acid change
NM_001083615.3:c.3290-5542A>G VV NP_001077084.2:p.=
NM_138995.4:c.3371-5542A>G VV NP_620482.3:p.=
NR_045682.1:n.3514-5542A>G
NR_045683.1:n.3514-5542A>G
NR_045684.1:n.3433-5542A>G
XM_006712299.2:c.3398-5542A>G XP_006712362.1:p.=
XM_011510654.1:c.3398-5542A>G XP_011508956.1:p.=
XM_011510655.1:c.3317-5542A>G XP_011508957.1:p.=
XM_011510656.1:c.2705-5542A>G XP_011508958.1:p.=
XM_011510657.1:c.2390-5542A>G XP_011508959.1:p.=
XM_011510658.1:c.2390-5542A>G XP_011508960.1:p.=
XM_006712299.4:c.3398-5542A>G XP_006712362.1:p.=
XM_011510654.3:c.3398-5542A>G XP_011508956.1:p.=
XM_011510655.3:c.3317-5542A>G XP_011508957.1:p.=
XM_011510656.3:c.2705-5542A>G XP_011508958.1:p.=
XM_011510657.3:c.2390-5542A>G XP_011508959.1:p.=
XM_011510658.3:c.2390-5542A>G XP_011508960.1:p.=
XM_024452713.1:c.2390-5542A>G XP_024308481.1:p.=
NM_001083615.4:c.3290-5542A>G VV NP_001077084.2:p.=
NM_138995.5:c.3371-5542A>G VV MANE Preferred NP_620482.3:p.=
NR_045682.2:n.3512-5542A>G
NR_045683.2:n.3512-5542A>G
NR_045684.2:n.3431-5542A>G
ENST00000317935.10:c.3290-5542A>G ENSP00000314650.6:p.=
ENST00000408978.8:c.3371-5542A>G ENSP00000386213.4:p.=
ENST00000409044.7:c.3290-5542A>G ENSP00000386497.3:p.=
ENST00000409940.6:n.3514-5542A>G
ENST00000438642.6:n.3514-5542A>G
ENST00000602629.1:n.2599-5542A>G