Linked Data
ClinVar Variation Id:
520352
dbSNP Id:
rs199498784
ExAC:
12:112891092 C / T
gnomAD v2:
12-112891092-C-T
gnomAD v3:
12-112453288-C-T
gnomAD v4:
12-112453288-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.112453288C>T , CM000674.2:g.112453288C>T | GRCh38 |
| NC_000012.11:g.112891092C>T , CM000674.1:g.112891092C>T | GRCh37 |
| NC_000012.10:g.111375475C>T | NCBI36 |
| NG_007459.1:g.39557C>T , LRG_614:g.39557C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000639857.2:c.426C>T | ENSP00000491593.2:p.Ser142= | |
| ENST00000685487.1:c.426C>T | ENSP00000508503.1:p.Ser142= | |
| ENST00000687906.1:c.426C>T | ENSP00000509536.1:p.Ser142= | |
| ENST00000688597.1:c.426C>T | ENSP00000510628.1:p.Ser142= | |
| ENST00000690210.1:c.426C>T | ENSP00000509272.1:p.Ser142= | |
| ENST00000692624.1:c.426C>T | ENSP00000508953.1:p.Ser142= | |
| ENST00000351677.7:c.426C>T MANE Select | ENSP00000340944.3:p.Ser142= | |
| ENST00000639857.1:c.426C>T | ENSP00000491593.1:p.Ser142= | |
| ENST00000351677.6:c.426C>T | ENSP00000340944.2:p.Ser142= | |
| ENST00000392597.5:c.426C>T | ENSP00000376376.1:p.Ser142= | |
| ENST00000635625.1:c.426C>T | ENSP00000489597.1:p.Ser142= | |
| NM_002834.3:c.426C>T , LRG_614t1:c.426C>T | NP_002825.3:p.Ser142= | |
| NM_080601.1:c.426C>T | NP_542168.1:p.Ser142= | |
| XM_006719526.1:c.426C>T | XP_006719589.1:p.Ser142= | |
| XM_006719527.1:c.426C>T | XP_006719590.1:p.Ser142= | |
| XM_011538613.1:c.423C>T | XP_011536915.1:p.Ser141= | |
| NM_001330437.1:c.426C>T | NP_001317366.1:p.Ser142= | |
| NM_002834.4:c.426C>T | NP_002825.3:p.Ser142= | |
| NM_080601.2:c.426C>T | NP_542168.1:p.Ser142= | |
| XM_011538613.2:c.423C>T | XP_011536915.1:p.Ser141= | |
| XM_017019722.1:c.423C>T | XP_016875211.1:p.Ser141= | |
| NM_001330437.2:c.426C>T | NP_001317366.1:p.Ser142= | |
| NM_001374625.1:c.423C>T | NP_001361554.1:p.Ser141= | |
| NM_002834.5:c.426C>T MANE Select | NP_002825.3:p.Ser142= | |
| NM_080601.3:c.426C>T | NP_542168.1:p.Ser142= |