Linked Data
ClinVar Variation Id:
345218
ClinVar RCV Id:
RCV000351595
dbSNP Id:
rs777749420
ExAC:
3:43743918 T / C
gnomAD v2:
3-43743918-T-C
gnomAD v4:
3-43702426-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.43702426T>C , CM000665.2:g.43702426T>C | GRCh38 |
| NC_000003.11:g.43743918T>C , CM000665.1:g.43743918T>C | GRCh37 |
| NC_000003.10:g.43718922T>C | NCBI36 |
| NG_007090.3:g.16544T>C | |
| NG_007090.5:g.16557T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000013894.3:c.*339T>C | ENSP00000013894.2:n.*339T>C | |
| ENST00000454293.2:c.222T>C | ENSP00000412014.2:p.Ser74= | |
| ENST00000458276.7:c.345T>C | ENSP00000390849.3:p.Ser115= | |
| ENST00000642351.1:c.222T>C | ENSP00000494478.1:p.Ser74= | |
| ENST00000643140.1:c.133+3065T>C | ENSP00000495588.1:n.133+3065T>C | |
| ENST00000643477.1:c.173T>C | ENSP00000496220.1:p.Val58Ala | |
| ENST00000643500.1:c.345T>C | ENSP00000494735.1:p.Ser115= | |
| ENST00000643520.1:n.393T>C | ||
| ENST00000644371.2:c.345T>C MANE Select | ENSP00000495778.1:p.Ser115= | |
| ENST00000646378.1:c.*395T>C | ENSP00000495826.1:n.*395T>C | |
| ENST00000646799.1:c.133+3065T>C | ENSP00000494829.1:n.133+3065T>C | |
| ENST00000649763.1:c.345T>C | ENSP00000497701.1:p.Ser115= | |
| ENST00000013894.2:c.*339T>C | ENSP00000013894.2:n.*339T>C | |
| ENST00000456453.5:c.222T>C | ENSP00000391582.1:p.Ser74= | |
| ENST00000458276.6:c.345T>C | ENSP00000390849.2:p.Ser115= | |
| NM_016006.4:c.345T>C | NP_057090.2:p.Ser115= | |
| XM_011533779.1:c.222T>C | XP_011532081.1:p.Ser74= | |
| XM_011533780.1:c.345T>C | XP_011532082.1:p.Ser115= | |
| XR_940447.1:n.402T>C | ||
| NM_001355186.1:c.345T>C | NP_001342115.1:p.Ser115= | |
| NM_001365649.1:c.222T>C | NP_001352578.1:p.Ser74= | |
| NM_001365650.1:c.345T>C | NP_001352579.1:p.Ser115= | |
| NM_016006.5:c.345T>C | NP_057090.2:p.Ser115= | |
| NR_158560.1:n.468T>C | ||
| NM_001355186.2:c.345T>C | NP_001342115.1:p.Ser115= | |
| NM_016006.6:c.345T>C MANE Select | NP_057090.2:p.Ser115= |