Linked Data
ClinVar Variation Id:
1159496
ClinVar RCV Id:
RCV001503277
dbSNP Id:
rs892319076
gnomAD v4:
11-2166761-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.2166761C>G , CM000673.2:g.2166761C>G | GRCh38 |
| NC_000011.9:g.2187991C>G , CM000673.1:g.2187991C>G | GRCh37 |
| NC_000011.8:g.2144567C>G | NCBI36 |
| NG_008128.1:g.10045G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000352909.8:c.849G>C MANE Select | ENSP00000325951.4:p.Thr283= | |
| ENST00000324155.8:c.*538G>C | ENSP00000325831.3:n.*538G>C | |
| ENST00000333684.9:c.696-212G>C | ENSP00000328814.6:n.696-212G>C | |
| ENST00000352909.7:c.849G>C | ENSP00000325951.3:p.Thr283= | |
| ENST00000381168.7:c.*569G>C | ENSP00000370560.3:n.*569G>C | |
| ENST00000381175.5:c.930G>C | ENSP00000370567.1:p.Thr310= | |
| ENST00000381178.5:c.942G>C | ENSP00000370571.1:p.Thr314= | |
| ENST00000412076.1:c.136-212G>C | ||
| ENST00000416223.5:c.143G>C | ||
| ENST00000461172.1:n.14G>C | ||
| ENST00000479437.5:n.398G>C | ||
| NM_000360.3:c.849G>C | NP_000351.2:p.Thr283= | |
| NM_199292.2:c.942G>C | NP_954986.2:p.Thr314= | |
| NM_199293.2:c.930G>C | NP_954987.2:p.Thr310= | |
| XM_011520335.1:c.861G>C | XP_011518637.1:p.Thr287= | |
| XM_011520335.2:c.861G>C | XP_011518637.1:p.Thr287= | |
| NM_000360.4:c.849G>C MANE Select | NP_000351.2:p.Thr283= | |
| NM_199292.3:c.942G>C | NP_954986.2:p.Thr314= | |
| NM_199293.3:c.930G>C | NP_954987.2:p.Thr310= |