Linked Data
ClinVar Variation Id:
1125258
ClinVar RCV Id:
RCV001456948
dbSNP Id:
rs1914464370
gnomAD v4:
16-89154204-A-G
MyVariant Identifiers:
chr16:g.89220612A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.89154204A>G , CM000678.2:g.89154204A>G | GRCh38 |
| NC_000016.9:g.89220612A>G , CM000678.1:g.89220612A>G | GRCh37 |
| NC_000016.8:g.87748113A>G | NCBI36 |
| NG_031961.1:g.65396A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000317447.9:c.1728A>G | ENSP00000320646.4:p.Ser576= | |
| ENST00000614302.5:c.1728A>G MANE Select | ENSP00000479130.1:p.Ser576= | |
| ENST00000649953.1:c.1938A>G | ENSP00000497456.1:p.Ser646= | |
| ENST00000317447.8:c.1728A>G | ENSP00000320646.4:p.Ser576= | |
| ENST00000378345.8:c.933A>G | ENSP00000367596.4:p.Ser311= | |
| ENST00000393145.5:n.6638A>G | ||
| ENST00000406948.7:c.1728A>G | ENSP00000384627.3:p.Ser576= | |
| ENST00000537116.5:n.854A>G | ||
| ENST00000537155.1:n.468A>G | ||
| ENST00000542688.5:c.*472A>G | ENSP00000446281.1:n.*472A>G | |
| ENST00000614302.4:c.1728A>G | ENSP00000479130.1:p.Ser576= | |
| NM_001127214.3:c.1728A>G | NP_001120686.1:p.Ser576= | |
| NM_001243279.2:c.1728A>G | NP_001230208.1:p.Ser576= | |
| NM_001284316.1:c.933A>G | NP_001271245.1:p.Ser311= | |
| NM_174917.4:c.1728A>G | NP_777577.2:p.Ser576= | |
| NR_045667.2:n.854A>G | ||
| NR_104293.1:n.2162A>G | ||
| XR_933239.1:n.2169A>G | ||
| XR_933240.1:n.2166A>G | ||
| XR_933241.1:n.1923A>G | ||
| NR_147928.1:n.2206A>G | ||
| NR_147929.1:n.1960A>G | ||
| XM_017023020.2:c.-3377A>G | XP_016878509.1:n.-3377A>G | |
| XM_024450187.1:c.933A>G | XP_024305955.1:p.Ser311= | |
| XR_001751864.2:n.1975A>G | ||
| XR_933240.3:n.2165A>G | ||
| NM_001127214.4:c.1728A>G | NP_001120686.1:p.Ser576= | |
| NM_001243279.3:c.1728A>G MANE Select | NP_001230208.1:p.Ser576= | |
| NM_001284316.2:c.933A>G | NP_001271245.1:p.Ser311= | |
| NM_174917.5:c.1728A>G | NP_777577.2:p.Ser576= | |
| NR_104293.2:n.2119A>G | ||
| NR_147928.2:n.2163A>G | ||
| NR_147929.2:n.1917A>G |