Linked Data
ClinVar Variation Id:
481367
dbSNP Id:
rs1401565860
gnomAD v2:
2-215657075-T-C
gnomAD v3:
2-214792351-T-C
gnomAD v4:
2-214792351-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.214792351T>C , CM000664.2:g.214792351T>C | GRCh38 |
| NC_000002.11:g.215657075T>C , CM000664.1:g.215657075T>C | GRCh37 |
| NC_000002.10:g.215365320T>C | NCBI36 |
| NG_012047.2:g.22354A>G | |
| NG_012047.3:g.22361A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260947.9:c.310A>G MANE Select | ENSP00000260947.4:p.Met104Val | |
| ENST00000421162.2:c.215+4710A>G | ENSP00000392245.2:n.215+4710A>G | |
| ENST00000613192.2:c.158+17061A>G | ENSP00000483275.2:n.158+17061A>G | |
| ENST00000613374.5:c.158+17061A>G | ENSP00000484464.1:n.158+17061A>G | |
| ENST00000613706.5:c.310A>G | ENSP00000484976.2:p.Met104Val | |
| ENST00000617164.5:c.253A>G | ENSP00000480470.1:p.Met85Val | |
| ENST00000619009.5:c.310A>G | ENSP00000482293.1:p.Met104Val | |
| ENST00000650978.1:c.152A>G | ||
| ENST00000260947.8:c.310A>G | ENSP00000260947.4:p.Met104Val | |
| ENST00000421162.1:c.215+4710A>G | ENSP00000392245.1:n.215+4710A>G | |
| ENST00000455743.5:c.215+4710A>G | ENSP00000412186.1:n.215+4710A>G | |
| ENST00000471787.1:n.260-10842A>G | ||
| ENST00000613192.1:c.73+17061A>G | ENSP00000483275.1:n.73+17061A>G | |
| ENST00000613374.4:c.158+17061A>G | ENSP00000484464.1:n.158+17061A>G | |
| ENST00000613706.4:c.215+4710A>G | ENSP00000484976.1:n.215+4710A>G | |
| ENST00000617164.4:c.253A>G | ENSP00000480470.1:p.Met85Val | |
| ENST00000619009.4:c.310A>G | ENSP00000482293.1:p.Met104Val | |
| ENST00000620057.4:c.310A>G | ENSP00000481988.1:p.Met104Val | |
| NM_000465.3:c.310A>G | NP_000456.2:p.Met104Val | |
| NM_001282543.1:c.253A>G | NP_001269472.1:p.Met85Val | |
| NM_001282545.1:c.215+4710A>G | NP_001269474.1:n.215+4710A>G | |
| NM_001282548.1:c.158+17061A>G | NP_001269477.1:n.158+17061A>G | |
| NM_001282549.1:c.310A>G | NP_001269478.1:p.Met104Val | |
| NR_104212.1:n.357+4710A>G | ||
| NR_104215.1:n.301-10842A>G | ||
| NR_104216.1:n.452A>G | ||
| XM_011511567.1:c.256A>G | XP_011509869.1:p.Met86Val | |
| XM_011511568.1:c.310A>G | XP_011509870.1:p.Met104Val | |
| XM_017004613.1:c.409A>G | XP_016860102.1:p.Met137Val | |
| XM_017004614.1:c.409A>G | XP_016860103.1:p.Met137Val | |
| XR_002959322.1:n.500A>G | ||
| NM_000465.4:c.310A>G MANE Select | NP_000456.2:p.Met104Val | |
| NM_001282543.2:c.253A>G | NP_001269472.1:p.Met85Val | |
| NM_001282545.2:c.215+4710A>G | NP_001269474.1:n.215+4710A>G | |
| NM_001282548.2:c.158+17061A>G | NP_001269477.1:n.158+17061A>G | |
| NM_001282549.2:c.310A>G | NP_001269478.1:p.Met104Val | |
| NR_104212.2:n.329+4710A>G | ||
| NR_104215.2:n.273-10842A>G | ||
| NR_104216.2:n.424A>G |