Linked Data
dbSNP Id:
rs1276240978
gnomAD v2:
6-36651938-C-T
gnomAD v3:
6-36684161-C-T
gnomAD v4:
6-36684161-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.36684161C>T , CM000668.2:g.36684161C>T | GRCh38 |
| NC_000006.11:g.36651938C>T , CM000668.1:g.36651938C>T | GRCh37 |
| NC_000006.10:g.36759916C>T | NCBI36 |
| NG_009364.1:g.10480C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000244741.10:c.60C>T MANE Select | ENSP00000244741.6:p.Arg20= | |
| ENST00000244741.9:c.60C>T | ENSP00000244741.5:p.Arg20= | |
| ENST00000373711.3:c.60C>T | ENSP00000362815.1:p.Arg20= | |
| ENST00000405375.5:c.60C>T | ENSP00000384849.1:p.Arg20= | |
| ENST00000448526.6:c.60C>T | ENSP00000409259.3:p.Arg20= | |
| ENST00000459970.1:n.254C>T | ||
| ENST00000478800.1:n.279C>T | ||
| ENST00000615513.4:c.60C>T | ENSP00000482768.1:p.Arg20= | |
| NM_000389.4:c.60C>T | NP_000380.1:p.Arg20= | |
| NM_001220777.1:c.60C>T | NP_001207706.1:p.Arg20= | |
| NM_001220778.1:c.60C>T | NP_001207707.1:p.Arg20= | |
| NM_001291549.1:c.162C>T | NP_001278478.1:p.Arg54= | |
| NM_078467.2:c.60C>T | NP_510867.1:p.Arg20= | |
| NM_000389.5:c.60C>T MANE Select | NP_000380.1:p.Arg20= | |
| NM_001220777.2:c.60C>T | NP_001207706.1:p.Arg20= | |
| NM_001220778.2:c.60C>T | NP_001207707.1:p.Arg20= | |
| NM_001291549.3:c.162C>T | NP_001278478.1:p.Arg54= | |
| NM_001374509.1:c.162C>T | NP_001361438.1:p.Arg54= | |
| NM_001374510.1:c.99C>T | NP_001361439.1:p.Arg33= | |
| NM_001374511.1:c.60C>T | NP_001361440.1:p.Arg20= | |
| NM_001374512.1:c.60C>T | NP_001361441.1:p.Arg20= | |
| NM_001374513.1:c.60C>T | NP_001361442.1:p.Arg20= | |
| NM_078467.3:c.60C>T | NP_510867.1:p.Arg20= |