Linked Data
ClinVar Variation Id:
2859879
ClinVar RCV Id:
RCV003635447
dbSNP Id:
rs1060501880
gnomAD v2:
16-89831327-G-T
gnomAD v4:
16-89764919-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.89764919G>T , CM000678.2:g.89764919G>T | GRCh38 |
| NC_000016.9:g.89831327G>T , CM000678.1:g.89831327G>T | GRCh37 |
| NC_000016.8:g.88358828G>T | NCBI36 |
| NG_011706.1:g.56739C>A , LRG_495:g.56739C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000561667.2:c.*1243C>A | ENSP00000512522.1:n.*1243C>A | |
| ENST00000564475.6:c.2749C>A | ENSP00000454977.2:p.Arg917= | |
| ENST00000567510.2:c.1448C>A | ENSP00000455969.1:n.1448C>A | |
| ENST00000568369.6:c.2749C>A | ENSP00000456829.1:p.Arg917= | |
| ENST00000696274.1:n.2710C>A | ||
| ENST00000696275.1:c.*1984C>A | ENSP00000512517.1:n.*1984C>A | |
| ENST00000696276.1:n.2792C>A | ||
| ENST00000696286.1:c.2749C>A | ENSP00000512523.1:p.Arg917= | |
| ENST00000696287.1:c.2749C>A | ENSP00000512524.1:p.Arg917= | |
| ENST00000696291.1:c.*2469C>A | ENSP00000512530.1:n.*2469C>A | |
| ENST00000389301.8:c.2749C>A MANE Select | ENSP00000373952.3:p.Arg917= | |
| ENST00000305699.15:n.121C>A | ||
| ENST00000389301.7:c.2749C>A | ENSP00000373952.3:p.Arg917= | |
| ENST00000561660.1:c.126C>A | ||
| ENST00000563318.1:c.155C>A | ||
| ENST00000563510.5:c.29C>A | ||
| ENST00000567988.5:c.86C>A | ||
| ENST00000568369.5:c.2749C>A | ENSP00000456829.1:p.Arg917= | |
| NM_000135.2:c.2749C>A , LRG_495t1:c.2749C>A | NP_000126.2:p.Arg917= | |
| NM_001286167.1:c.2749C>A | NP_001273096.1:p.Arg917= | |
| XM_005256294.3:c.2749C>A | XP_005256351.1:p.Arg917= | |
| XM_011522945.1:c.2749C>A | XP_011521247.1:p.Arg917= | |
| XM_011522946.1:c.1726C>A | XP_011521248.1:p.Arg576= | |
| XM_011522947.1:c.1726C>A | XP_011521249.1:p.Arg576= | |
| XR_933244.1:n.2792C>A | ||
| XR_933245.1:n.2792C>A | ||
| XR_933246.1:n.2792C>A | ||
| NM_000135.3:c.2749C>A | NP_000126.2:p.Arg917= | |
| NM_001286167.2:c.2749C>A | NP_001273096.1:p.Arg917= | |
| XM_005256294.4:c.2749C>A | XP_005256351.1:p.Arg917= | |
| XM_011522945.2:c.2749C>A | XP_011521247.1:p.Arg917= | |
| XM_011522946.3:c.1726C>A | XP_011521248.1:p.Arg576= | |
| XM_011522947.2:c.1726C>A | XP_011521249.1:p.Arg576= | |
| XM_017023044.2:c.2749C>A | XP_016878533.1:p.Arg917= | |
| XM_017023045.1:c.2749C>A | XP_016878534.1:p.Arg917= | |
| XM_024450189.1:c.1726C>A | XP_024305957.1:p.Arg576= | |
| XR_001751866.1:n.2792C>A | ||
| XR_933244.2:n.2792C>A | ||
| XR_933245.2:n.2792C>A | ||
| XR_933247.2:n.2921C>A | ||
| NM_000135.4:c.2749C>A MANE Select | NP_000126.2:p.Arg917= | |
| NM_001286167.3:c.2749C>A | NP_001273096.1:p.Arg917= |