Canonical Allele Identifier: CA794649350

Linked Data

dbSNP Id: rs1313331240

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.38829928G>A , CM000666.2:g.38829928G>A GRCh38
NC_000004.11:g.38831549G>A , CM000666.1:g.38831549G>A GRCh37
NC_000004.10:g.38507944G>A NCBI36
NG_028087.1:g.31890C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000381950.2:c.-64-391C>T (TLR6) ENSP00000371376.1:n.-64-391C>T
ENST00000508254.6:c.-64-391C>T (TLR6) MANE Select ENSP00000424718.2:n.-64-391C>T
ENST00000436693.6:c.-64-391C>T (TLR6) ENSP00000389600.2:n.-64-391C>T
ENST00000506146.5:c.-352-24735C>T (TLR1) ENSP00000423725.1:n.-352-24735C>T
ENST00000508254.5:c.-64-391C>T (TLR6) ENSP00000424718.1:n.-64-391C>T
ENST00000514655.1:c.-64-391C>T (TLR6) ENSP00000423326.1:n.-64-391C>T
NM_006068.4:c.-64-391C>T (TLR6) NP_006059.2:n.-64-391C>T
XM_005262637.3:c.-64-391C>T (TLR6) XP_005262694.1:n.-64-391C>T
XM_011513612.1:c.-64-391C>T (TLR6) XP_011511914.1:n.-64-391C>T
XM_011513613.1:c.-64-391C>T (TLR6) XP_011511915.1:n.-64-391C>T
XM_011513614.1:c.-64-391C>T (TLR6) XP_011511916.1:n.-64-391C>T
XM_005262637.5:c.-64-391C>T (TLR6) XP_005262694.1:n.-64-391C>T
XM_011513613.3:c.-64-391C>T (TLR6) XP_011511915.1:n.-64-391C>T
XM_011513614.3:c.-64-391C>T (TLR6) XP_011511916.1:n.-64-391C>T
XM_024453873.1:c.-64-391C>T (TLR6) XP_024309641.1:n.-64-391C>T
NM_006068.5:c.-64-391C>T (TLR6) MANE Select NP_006059.2:n.-64-391C>T
NM_001394553.1:c.-64-391C>T (TLR6) NP_001381482.1:n.-64-391C>T