Linked Data
dbSNP Id:
rs2569190
gnomAD v2:
5-140012916-A-G
gnomAD v3:
5-140633331-A-G
gnomAD v4:
5-140633331-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.140633331A>G , CM000667.2:g.140633331A>G | GRCh38 |
| NC_000005.9:g.140012916A>G , CM000667.1:g.140012916A>G | GRCh37 |
| NC_000005.8:g.139993100A>G | NCBI36 |
| NG_023178.1:g.5371T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000498971.7:c.-121-139T>C (CD14) | ENSP00000426543.2:n.-121-139T>C | |
| ENST00000512545.2:c.-221-39T>C (CD14) | ENSP00000425447.2:n.-221-39T>C | |
| ENST00000519715.2:c.-121-139T>C (CD14) | ENSP00000430884.2:n.-121-139T>C | |
| ENST00000302014.10:c.-260T>C (CD14) | ENSP00000304236.6:n.-260T>C | |
| ENST00000401743.6:c.-221-39T>C (CD14) | ENSP00000385519.2:n.-221-39T>C | |
| ENST00000498971.6:c.-121-139T>C (CD14) | ENSP00000426543.1:n.-121-139T>C | |
| ENST00000512545.1:c.-221-39T>C (CD14) | ENSP00000425447.1:n.-221-39T>C | |
| ENST00000519715.1:c.-121-139T>C (CD14) | ENSP00000430884.1:n.-121-139T>C | |
| NM_000591.3:c.-260T>C (CD14) | NP_000582.1:n.-260T>C | |
| NM_001040021.2:c.-121-139T>C (CD14) | NP_001035110.1:n.-121-139T>C | |
| NM_001174104.1:c.-221-39T>C (CD14) | NP_001167575.1:n.-221-39T>C | |
| NM_001174105.1:c.-121-139T>C (CD14) | NP_001167576.1:n.-121-139T>C | |
| XM_011537665.1:c.-129-8334A>G (TMCO6) | XP_011535967.1:n.-129-8334A>G | |
| XM_011537665.2:c.-129-8334A>G (TMCO6) | XP_011535967.1:n.-129-8334A>G | |
| NM_001040021.3:c.-121-139T>C (CD14) | NP_001035110.1:n.-121-139T>C | |
| NM_001174105.2:c.-121-139T>C (CD14) | NP_001167576.1:n.-121-139T>C | |
| NM_001174104.2:c.-221-39T>C (CD14) | NP_001167575.1:n.-221-39T>C |