LDH info

Canonical Allele Identifier: CA273899
Gene: LAMB3 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 188740
ClinVar RCV Id: RCV000169049
dbSNP Id: rs371267954

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209650120T>C , CM000663.2:g.209650120T>C GRCh38
NC_000001.10:g.209823465T>C , CM000663.1:g.209823465T>C GRCh37
NC_000001.9:g.207890088T>C NCBI36
NG_007116.1:g.7356A>G

Transcript Alleles

HGVS Amino-acid change
NM_000228.2:c.29-2A>G VV NP_000219.2:p.=
NM_001017402.1:c.29-2A>G VV NP_001017402.1:p.=
NM_001127641.1:c.29-2A>G VV NP_001121113.1:p.=
XM_005273124.3:c.29-2A>G XP_005273181.1:p.=
XM_005273124.4:c.29-2A>G XP_005273181.1:p.=
XM_017001272.2:c.29-2A>G XP_016856761.1:p.=
NM_000228.3:c.29-2A>G VV MANE Preferred NP_000219.2:p.=
ENST00000356082.8:c.29-2A>G ENSP00000348384.3:p.=
ENST00000367030.7:c.29-2A>G ENSP00000355997.3:p.=
ENST00000391911.5:c.29-2A>G ENSP00000375778.1:p.=
ENST00000415782.1:c.29-2A>G ENSP00000388960.1:p.=