LDH info

Canonical Allele Identifier: CA257286
Gene: LAMB3 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 14551
ClinVar RCV Id: RCV000015652
dbSNP Id: rs587776813

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209633136A>G , CM000663.2:g.209633136A>G GRCh38
NC_000001.10:g.209806481A>G , CM000663.1:g.209806481A>G GRCh37
NC_000001.9:g.207873104A>G NCBI36
NG_007116.1:g.24340T>C

Transcript Alleles

HGVS Amino-acid change
NM_000228.2:c.565-3T>C VV NP_000219.2:p.=
NM_001017402.1:c.565-3T>C VV NP_001017402.1:p.=
NM_001127641.1:c.565-3T>C VV NP_001121113.1:p.=
XM_005273124.3:c.565-3T>C XP_005273181.1:p.=
XM_005273124.4:c.565-3T>C XP_005273181.1:p.=
XM_017001272.2:c.373-3T>C XP_016856761.1:p.=
NM_000228.3:c.565-3T>C VV MANE Preferred NP_000219.2:p.=
ENST00000356082.8:c.565-3T>C ENSP00000348384.3:p.=
ENST00000367030.7:c.565-3T>C ENSP00000355997.3:p.=
ENST00000391911.5:c.565-3T>C ENSP00000375778.1:p.=