Canonical Allele Identifier: CA1586825366

Linked Data

dbSNP Id: rs1756680194

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140633321A>G , CM000667.2:g.140633321A>G GRCh38
NC_000005.9:g.140012906A>G , CM000667.1:g.140012906A>G GRCh37
NC_000005.8:g.139993090A>G NCBI36
NG_023178.1:g.5381T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000498971.7:c.-121-129T>C (CD14) ENSP00000426543.2:n.-121-129T>C
ENST00000512545.2:c.-221-29T>C (CD14) ENSP00000425447.2:n.-221-29T>C
ENST00000519715.2:c.-121-129T>C (CD14) ENSP00000430884.2:n.-121-129T>C
ENST00000302014.10:c.-250T>C (CD14) ENSP00000304236.6:n.-250T>C
ENST00000401743.6:c.-221-29T>C (CD14) ENSP00000385519.2:n.-221-29T>C
ENST00000498971.6:c.-121-129T>C (CD14) ENSP00000426543.1:n.-121-129T>C
ENST00000512545.1:c.-221-29T>C (CD14) ENSP00000425447.1:n.-221-29T>C
ENST00000519715.1:c.-121-129T>C (CD14) ENSP00000430884.1:n.-121-129T>C
NM_000591.3:c.-250T>C (CD14) NP_000582.1:n.-250T>C
NM_001040021.2:c.-121-129T>C (CD14) NP_001035110.1:n.-121-129T>C
NM_001174104.1:c.-221-29T>C (CD14) NP_001167575.1:n.-221-29T>C
NM_001174105.1:c.-121-129T>C (CD14) NP_001167576.1:n.-121-129T>C
XM_011537665.1:c.-129-8344A>G (TMCO6) XP_011535967.1:n.-129-8344A>G
XM_011537665.2:c.-129-8344A>G (TMCO6) XP_011535967.1:n.-129-8344A>G
NM_001040021.3:c.-121-129T>C (CD14) NP_001035110.1:n.-121-129T>C
NM_001174105.2:c.-121-129T>C (CD14) NP_001167576.1:n.-121-129T>C
NM_001174104.2:c.-221-29T>C (CD14) NP_001167575.1:n.-221-29T>C