Linked Data
ClinVar Variation Id:
378091
dbSNP Id:
rs147615538
ExAC:
18:2951197 G / A
gnomAD v2:
18-2951197-G-A
gnomAD v3:
18-2951199-G-A
gnomAD v4:
18-2951199-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.2951199G>A , CM000680.2:g.2951199G>A | GRCh38 |
| NC_000018.9:g.2951197G>A , CM000680.1:g.2951197G>A | GRCh37 |
| NC_000018.8:g.2941197G>A | NCBI36 |
| NG_007507.1:g.65749C>T , LRG_174:g.65749C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261596.9:c.446C>T | ENSP00000261596.4:p.Pro149Leu | |
| ENST00000584915.2:c.557C>T | ENSP00000463810.2:p.Pro186Leu | |
| ENST00000697039.1:c.446C>T | ENSP00000513061.1:p.Pro149Leu | |
| ENST00000697040.1:c.446C>T | ENSP00000513062.1:p.Pro149Leu | |
| ENST00000697042.1:c.446C>T | ENSP00000513064.1:p.Pro149Leu | |
| ENST00000697043.1:c.446C>T | ENSP00000513065.1:p.Pro149Leu | |
| ENST00000677752.1:c.446C>T MANE Select | ENSP00000504857.1:p.Pro149Leu | |
| ENST00000261596.8:c.446C>T | ENSP00000261596.4:p.Pro149Leu | |
| ENST00000584294.1:c.446C>T | ENSP00000463026.1:p.Pro149Leu | |
| NM_014646.2:c.446C>T , LRG_174t1:c.446C>T | NP_055461.1:p.Pro149Leu | |
| XM_005258177.3:c.557C>T | XP_005258234.1:p.Pro186Leu | |
| XM_005258178.2:c.446C>T | XP_005258235.1:p.Pro149Leu | |
| XM_005258179.3:c.446C>T | XP_005258236.1:p.Pro149Leu | |
| XR_935074.1:n.575C>T | ||
| XM_005258177.4:c.557C>T | XP_005258234.1:p.Pro186Leu | |
| XM_005258178.3:c.446C>T | XP_005258235.1:p.Pro149Leu | |
| XM_005258179.5:c.446C>T | XP_005258236.1:p.Pro149Leu | |
| XM_017026098.1:c.446C>T | XP_016881587.1:p.Pro149Leu | |
| XM_017026099.1:c.446C>T | XP_016881588.1:p.Pro149Leu | |
| XR_935074.2:n.620C>T | ||
| NM_001375808.1:c.446C>T | NP_001362737.1:p.Pro149Leu | |
| NM_001375809.1:c.446C>T | NP_001362738.1:p.Pro149Leu | |
| NM_001375808.2:c.446C>T MANE Select | NP_001362737.1:p.Pro149Leu |