Linked Data
ClinVar Variation Id:
237755
ClinVar RCV Id:
RCV000233360
RCV001149347
RCV001149348
RCV001149346
RCV001149345
RCV003144169
RCV004020749
RCV004554754
dbSNP Id:
rs200312817
ExAC:
3:121981070 A / G
gnomAD v2:
3-121981070-A-G
gnomAD v3:
3-122262223-A-G
gnomAD v4:
3-122262223-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.122262223A>G , CM000665.2:g.122262223A>G | GRCh38 |
| NC_000003.11:g.121981070A>G , CM000665.1:g.121981070A>G | GRCh37 |
| NC_000003.10:g.123463760A>G | NCBI36 |
| NG_009058.1:g.83541A>G | |
| NG_009058.2:g.83556A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000490131.7:c.1188A>G | ENSP00000418685.2:p.Thr396= | |
| ENST00000498619.4:c.1188A>G | ENSP00000420194.1:p.Thr396= | |
| ENST00000638421.1:c.1188A>G | ENSP00000492190.1:p.Thr396= | |
| ENST00000639785.2:c.1188A>G MANE Select | ENSP00000491584.2:p.Thr396= | |
| ENST00000490131.5:c.1188A>G | ENSP00000418685.1:p.Thr396= | |
| ENST00000498619.2:c.1188A>G | ENSP00000420194.1:p.Thr396= | |
| NM_000388.3:c.1188A>G | NP_000379.2:p.Thr396= | |
| NM_001178065.1:c.1188A>G | NP_001171536.1:p.Thr396= | |
| XM_005247836.2:c.1188A>G | XP_005247893.1:p.Thr396= | |
| XM_005247837.2:c.705A>G | XP_005247894.1:p.Thr235= | |
| XM_006713789.2:c.1188A>G | XP_006713852.1:p.Thr396= | |
| XM_011513237.1:c.1188A>G | XP_011511539.1:p.Thr396= | |
| XM_011513238.1:c.1188A>G | XP_011511540.1:p.Thr396= | |
| XM_011513239.1:c.600A>G | XP_011511541.1:p.Thr200= | |
| XM_006713789.3:c.1188A>G | XP_006713852.1:p.Thr396= | |
| XM_017007324.1:c.1188A>G | XP_016862813.1:p.Thr396= | |
| XM_017007325.1:c.1188A>G | XP_016862814.1:p.Thr396= | |
| NM_000388.4:c.1188A>G MANE Select | NP_000379.3:p.Thr396= | |
| NM_001178065.2:c.1188A>G | NP_001171536.2:p.Thr396= |