Linked Data
ClinVar Variation Id:
3014026
ClinVar RCV Id:
RCV003873601
dbSNP Id:
rs794727767
gnomAD v2:
11-103091450-T-C
gnomAD v3:
11-103220721-T-C
gnomAD v4:
11-103220721-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.103220721T>C , CM000673.2:g.103220721T>C | GRCh38 |
| NC_000011.9:g.103091450T>C , CM000673.1:g.103091450T>C | GRCh37 |
| NC_000011.8:g.102596660T>C | NCBI36 |
| NG_016423.1:g.116291T>C | |
| NG_016423.2:g.116291T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650373.2:c.9045T>C MANE Plus Clinical | ENSP00000497174.1:p.Asp3015= | |
| ENST00000375735.7:c.9045T>C MANE Select | ENSP00000364887.2:p.Asp3015= | |
| ENST00000650373.1:c.9045T>C | ENSP00000497174.1:p.Asp3015= | |
| ENST00000334267.11:c.2205+86302T>C | ENSP00000334021.7:n.2205+86302T>C | |
| ENST00000375735.6:c.9045T>C | ENSP00000364887.2:p.Asp3015= | |
| ENST00000398093.7:c.9045T>C | ENSP00000381167.3:p.Asp3015= | |
| NM_001080463.1:c.9045T>C | NP_001073932.1:p.Asp3015= | |
| NM_001377.2:c.9045T>C | NP_001368.2:p.Asp3015= | |
| XM_006718903.2:c.9024T>C | XP_006718966.1:p.Asp3008= | |
| XM_017018291.1:c.9045T>C | XP_016873780.1:p.Asp3015= | |
| XM_017018292.1:c.8427T>C | XP_016873781.1:p.Asp2809= | |
| NM_001377.3:c.9045T>C MANE Select | NP_001368.2:p.Asp3015= | |
| NM_001080463.2:c.9045T>C MANE Plus Clinical | NP_001073932.1:p.Asp3015= |