Linked Data
ClinVar Variation Id:
67180
dbSNP Id:
rs199472899
ExAC:
7:150649787 G / A
gnomAD v2:
7-150649787-G-A
gnomAD v3:
7-150952699-G-A
gnomAD v4:
7-150952699-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.150952699G>A , CM000669.2:g.150952699G>A | GRCh38 |
| NC_000007.13:g.150649787G>A , CM000669.1:g.150649787G>A | GRCh37 |
| NC_000007.12:g.150280720G>A | NCBI36 |
| NG_008916.1:g.30228C>T , LRG_288:g.30228C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000461280.2:n.581C>T | ||
| ENST00000684116.1:n.176C>T | ||
| ENST00000684241.1:n.2116C>T | ||
| ENST00000262186.10:c.1283C>T MANE Select | ENSP00000262186.5:p.Ser428Leu | |
| ENST00000330883.9:c.263C>T | ENSP00000328531.4:p.Ser88Leu | |
| ENST00000262186.9:c.1283C>T | ENSP00000262186.5:p.Ser428Leu | |
| ENST00000330883.8:c.263C>T | ENSP00000328531.4:p.Ser88Leu | |
| ENST00000430723.4:c.935C>T | ENSP00000387657.4:p.Ser312Leu | |
| ENST00000461280.1:n.570C>T | ||
| ENST00000473610.5:n.588C>T | ||
| ENST00000532957.5:n.1506C>T | ||
| NM_000238.3:c.1283C>T , LRG_288t1:c.1283C>T | NP_000229.1:p.Ser428Leu | |
| NM_001204798.1:c.263C>T | NP_001191727.1:p.Ser88Leu | |
| NM_172056.2:c.1283C>T , LRG_288t2:c.1283C>T | NP_742053.1:p.Ser428Leu | |
| NM_172057.2:c.263C>T , LRG_288t3:c.263C>T | NP_742054.1:p.Ser88Leu | |
| XM_011516185.1:c.983C>T | XP_011514487.1:p.Ser328Leu | |
| XM_011516186.1:c.1283C>T | XP_011514488.1:p.Ser428Leu | |
| XM_011516185.2:c.983C>T | XP_011514487.1:p.Ser328Leu | |
| XM_011516186.3:c.1283C>T | XP_011514488.1:p.Ser428Leu | |
| XM_017012195.1:c.1133C>T | XP_016867684.1:p.Ser378Leu | |
| XM_017012196.1:c.1106C>T | XP_016867685.1:p.Ser369Leu | |
| NM_000238.4:c.1283C>T MANE Select | NP_000229.1:p.Ser428Leu | |
| NM_001204798.2:c.263C>T | NP_001191727.1:p.Ser88Leu | |
| NM_172057.3:c.263C>T | NP_742054.1:p.Ser88Leu |