LDH info

Canonical Allele Identifier: CA11644229
Gene: TLR6 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1039559

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.38829975G>A , CM000666.2:g.38829975G>A GRCh38
NC_000004.11:g.38831596G>A , CM000666.1:g.38831596G>A GRCh37
NC_000004.10:g.38507991G>A NCBI36
NG_028087.1:g.31843C>T

Transcript Alleles

HGVS Amino-acid change
NM_006068.4:c.-64-438C>T VV NP_006059.2:p.=
XM_005262637.3:c.-64-438C>T XP_005262694.1:p.=
XM_011513612.1:c.-64-438C>T XP_011511914.1:p.=
XM_011513613.1:c.-64-438C>T XP_011511915.1:p.=
XM_011513614.1:c.-64-438C>T XP_011511916.1:p.=
XM_005262637.5:c.-64-438C>T XP_005262694.1:p.=
XM_011513613.3:c.-64-438C>T XP_011511915.1:p.=
XM_011513614.3:c.-64-438C>T XP_011511916.1:p.=
XM_024453873.1:c.-64-438C>T XP_024309641.1:p.=
ENST00000436693.6:c.-64-438C>T ENSP00000389600.2:p.=
ENST00000506146.5:c.-352-24782C>T ENSP00000423725.1:p.=
ENST00000508254.5:c.-64-438C>T ENSP00000424718.1:p.=
ENST00000514655.1:c.-64-438C>T ENSP00000423326.1:p.=