LDH info

Canonical Allele Identifier: CA257280
Gene: LAMB3 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 14546
ClinVar RCV Id: RCV000015647
dbSNP Id: rs121912485

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209618555G>A , CM000663.2:g.209618555G>A GRCh38
NC_000001.10:g.209791900G>A , CM000663.1:g.209791900G>A GRCh37
NC_000001.9:g.207858523G>A NCBI36
NG_007116.1:g.38921C>T

Transcript Alleles

HGVS Amino-acid change
NM_000228.2:c.2806C>T VV NP_000219.2:p.Gln936Ter
NM_001017402.1:c.2806C>T VV NP_001017402.1:p.Gln936Ter
NM_001127641.1:c.2806C>T VV NP_001121113.1:p.Gln936Ter
XM_005273124.3:c.2806C>T XP_005273181.1:p.Gln936Ter
XM_005273124.4:c.2806C>T XP_005273181.1:p.Gln936Ter
XM_017001272.2:c.2614C>T XP_016856761.1:p.Gln872Ter
NM_000228.3:c.2806C>T VV MANE Preferred NP_000219.2:p.Gln936Ter
ENST00000356082.8:c.2806C>T ENSP00000348384.3:p.Gln936Ter
ENST00000367030.7:c.2806C>T ENSP00000355997.3:p.Gln936Ter
ENST00000391911.5:c.2806C>T ENSP00000375778.1:p.Gln936Ter
ENST00000455193.1:c.13C>T ENSP00000398683.1:p.Gln5Ter