Linked Data
ClinVar Variation Id:
9115
dbSNP Id:
rs137852668
gnomAD v4:
11-68906103-C-T
PubMed:
PMID:11528396
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.68906103C>T , CM000673.2:g.68906103C>T | GRCh38 |
| NC_000011.9:g.68673571C>T , CM000673.1:g.68673571C>T | GRCh37 |
| NC_000011.8:g.68430147C>T | NCBI36 |
| NG_007976.1:g.7253C>T , LRG_250:g.7253C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000255078.8:c.121C>T MANE Select | ENSP00000255078.4:p.Gln41Ter | |
| ENST00000539224.2:c.84C>T | ||
| ENST00000674583.1:c.84C>T | ||
| ENST00000674597.1:c.35C>T | ||
| ENST00000674729.1:n.64C>T | ||
| ENST00000674955.1:c.121C>T | ENSP00000502463.1:p.Gln41Ter | |
| ENST00000675142.1:n.84C>T | ||
| ENST00000675469.1:c.35C>T | ||
| ENST00000675615.1:c.121C>T | ENSP00000502413.1:p.Gln41Ter | |
| ENST00000675674.1:n.84C>T | ||
| ENST00000675800.1:n.66C>T | ||
| ENST00000675873.1:c.84C>T | ||
| ENST00000676173.1:n.161C>T | ||
| ENST00000676228.1:c.121C>T | ENSP00000502375.1:p.Gln41Ter | |
| ENST00000255078.7:c.121C>T | ENSP00000255078.3:p.Gln41Ter | |
| ENST00000539224.1:c.121C>T | ENSP00000440465.1:p.Gln41Ter | |
| ENST00000544541.1:c.87-2042C>T | ENSP00000443343.1:n.87-2042C>T | |
| ENST00000545146.1:c.121C>T | ENSP00000456366.1:p.Gln41Ter | |
| NM_002180.2:c.121C>T , LRG_250t1:c.121C>T | NP_002171.2:p.Gln41Ter | |
| XM_005273974.2:c.-895C>T | XP_005274031.1:n.-895C>T | |
| XM_005273976.1:c.121C>T | XP_005274033.1:p.Gln41Ter | |
| XR_247198.1:n.223C>T | ||
| XR_949903.1:n.223C>T | ||
| XM_005273976.2:c.121C>T | XP_005274033.1:p.Gln41Ter | |
| XM_017017669.2:c.-793C>T | XP_016873158.1:n.-793C>T | |
| XM_017017671.2:c.121C>T | XP_016873160.1:p.Gln41Ter | |
| XR_949903.3:n.219C>T | ||
| NM_002180.3:c.121C>T MANE Select | NP_002171.2:p.Gln41Ter |