Linked Data
ClinVar Variation Id:
138772
dbSNP Id:
rs371431444
ExAC:
15:89872020 G / A
gnomAD v2:
15-89872020-G-A
gnomAD v3:
15-89328789-G-A
gnomAD v4:
15-89328789-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.89328789G>A , CM000677.2:g.89328789G>A | GRCh38 |
| NC_000015.9:g.89872020G>A , CM000677.1:g.89872020G>A | GRCh37 |
| NC_000015.8:g.87673024G>A | NCBI36 |
| NG_008218.1:g.11007C>T | |
| NG_008218.2:g.11007C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000636937.2:c.1066C>T | ENSP00000516154.1:p.Leu356= | |
| ENST00000268124.11:c.1066C>T MANE Select | ENSP00000268124.5:p.Leu356= | |
| ENST00000530292.3:c.667C>T | ENSP00000432885.2:p.Leu223= | |
| ENST00000635986.2:c.1066C>T | ENSP00000490653.2:p.Leu356= | |
| ENST00000636774.1:c.1066C>T | ENSP00000489799.1:p.Leu356= | |
| ENST00000637264.1:c.138C>T | ||
| ENST00000666746.1:c.723C>T | ||
| ENST00000672071.1:n.1264C>T | ||
| ENST00000672923.2:n.63C>T | ||
| ENST00000268124.9:c.1066C>T | ENSP00000268124.5:p.Leu356= | |
| ENST00000442287.6:c.1066C>T | ENSP00000399851.2:p.Leu356= | |
| ENST00000631044.2:c.*449C>T | ENSP00000486730.1:n.*449C>T | |
| NM_001126131.1:c.1066C>T | NP_001119603.1:p.Leu356= | |
| NM_002693.2:c.1066C>T | NP_002684.1:p.Leu356= | |
| NM_001126131.2:c.1066C>T | NP_001119603.1:p.Leu356= | |
| NM_002693.3:c.1066C>T MANE Select | NP_002684.1:p.Leu356= |