Linked Data
ClinVar Variation Id:
1116991
ClinVar RCV Id:
RCV001445556
dbSNP Id:
rs1369827088
gnomAD v2:
16-56904009-T-C
gnomAD v3:
16-56870097-T-C
gnomAD v4:
16-56870097-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.56870097T>C , CM000678.2:g.56870097T>C | GRCh38 |
| NC_000016.9:g.56904009T>C , CM000678.1:g.56904009T>C | GRCh37 |
| NC_000016.8:g.55461510T>C | NCBI36 |
| NG_009386.1:g.9891T>C | |
| NG_009386.2:g.9891T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000563236.6:c.603T>C MANE Select | ENSP00000456149.2:p.Gly201= | |
| ENST00000262502.5:c.600T>C | ENSP00000262502.5:p.Gly200= | |
| ENST00000438926.6:c.603T>C | ENSP00000402152.2:p.Gly201= | |
| ENST00000563236.5:c.603T>C | ENSP00000456149.1:p.Gly201= | |
| ENST00000566786.5:c.600T>C | ENSP00000457552.1:p.Gly200= | |
| NM_000339.2:c.603T>C | NP_000330.2:p.Gly201= | |
| NM_001126107.1:c.600T>C | NP_001119579.1:p.Gly200= | |
| NM_001126108.1:c.603T>C | NP_001119580.1:p.Gly201= | |
| XM_005256119.1:c.600T>C | XP_005256176.1:p.Gly200= | |
| XM_005256119.2:c.600T>C | XP_005256176.1:p.Gly200= | |
| NM_000339.3:c.603T>C | NP_000330.3:p.Gly201= | |
| NM_001126107.2:c.600T>C | NP_001119579.2:p.Gly200= | |
| NM_001126108.2:c.603T>C MANE Select | NP_001119580.2:p.Gly201= |