LDH info

Canonical Allele Identifier: CA10810953
Gene: TGFBR3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs284875

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.91705151A>G , CM000663.2:g.91705151A>G GRCh38
NC_000001.10:g.92170708A>G , CM000663.1:g.92170708A>G GRCh37
NC_000001.9:g.91943296A>G NCBI36
NG_027757.1:g.205852T>C

Transcript Alleles

HGVS Amino-acid change
NM_001195683.1:c.2284+3512T>C VV NP_001182612.1:p.=
NM_001195684.1:c.2284+3512T>C VV NP_001182613.1:p.=
NM_003243.4:c.2287+3512T>C VV NP_003234.2:p.=
NR_036634.1:n.2899+3512T>C
XM_006710867.1:c.2287+3512T>C XP_006710930.1:p.=
XM_006710868.1:c.2287+3512T>C XP_006710931.1:p.=
XM_011542058.1:c.1621+3512T>C XP_011540360.1:p.=
XM_006710867.2:c.2287+3512T>C XP_006710930.1:p.=
NM_003243.5:c.2287+3512T>C VV MANE Preferred NP_003234.2:p.=
NM_001195683.2:c.2284+3512T>C VV NP_001182612.1:p.=
NR_036634.2:n.2771+3512T>C
ENST00000212355.8:c.2287+3512T>C ENSP00000212355.4:p.=
ENST00000370399.6:c.2284+3512T>C ENSP00000359426.2:p.=
ENST00000465892.6:c.2284+3512T>C ENSP00000432638.1:p.=
ENST00000470600.1:n.242+3512T>C
ENST00000525962.5:c.2287+3512T>C ENSP00000436127.1:p.=
ENST00000532540.5:c.*2234+3512T>C ENSP00000434994.1:p.=
ENST00000533089.5:c.*2005+3512T>C ENSP00000433477.1:p.=