Linked Data
ClinVar Variation Id:
498870
dbSNP Id:
rs900061092
gnomAD v2:
11-61160791-A-T
gnomAD v3:
11-61393319-A-T
gnomAD v4:
11-61393319-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.61393319A>T , CM000673.2:g.61393319A>T | GRCh38 |
| NC_000011.9:g.61160791A>T , CM000673.1:g.61160791A>T | GRCh37 |
| NC_000011.8:g.60917367A>T | NCBI36 |
| NG_032976.1:g.5960A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000334888.10:c.123A>T | ENSP00000334844.5:p.Ile41= | |
| ENST00000544795.6:n.400A>T | ||
| ENST00000684926.1:n.139A>T | ||
| ENST00000688959.1:c.-137A>T | ENSP00000509213.1:n.-137A>T | |
| ENST00000690736.1:c.123A>T | ENSP00000508542.1:p.Ile41= | |
| ENST00000515837.7:c.123A>T MANE Select | ENSP00000440638.1:p.Ile41= | |
| ENST00000334888.9:c.123A>T | ENSP00000334844.5:p.Ile41= | |
| ENST00000398979.7:c.-61A>T | ENSP00000381950.3:n.-61A>T | |
| ENST00000515837.6:c.123A>T | ENSP00000440638.1:p.Ile41= | |
| ENST00000541473.1:n.137A>T | ||
| ENST00000544795.5:n.139A>T | ||
| NM_001173990.2:c.123A>T | NP_001167461.1:p.Ile41= | |
| NM_001173991.2:c.123A>T | NP_001167462.1:p.Ile41= | |
| NM_016499.5:c.-61A>T | NP_057583.2:n.-61A>T | |
| XM_005274039.3:c.-61A>T | XP_005274096.1:n.-61A>T | |
| NM_001330285.1:c.-61A>T | NP_001317214.1:n.-61A>T | |
| XM_005274039.4:c.-61A>T | XP_005274096.1:n.-61A>T | |
| NM_001173990.3:c.123A>T MANE Select | NP_001167461.1:p.Ile41= | |
| NM_001173991.3:c.123A>T | NP_001167462.1:p.Ile41= | |
| NM_001330285.2:c.-61A>T | NP_001317214.1:n.-61A>T | |
| NM_016499.6:c.-61A>T | NP_057583.2:n.-61A>T |