Linked Data
ClinVar Variation Id:
1091134
ClinVar RCV Id:
RCV001410556
dbSNP Id:
rs767852112
ExAC:
1:53676601 C / T
gnomAD v2:
1-53676601-C-T
gnomAD v3:
1-53210929-C-T
gnomAD v4:
1-53210929-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.53210929C>T , CM000663.2:g.53210929C>T | GRCh38 |
| NC_000001.10:g.53676601C>T , CM000663.1:g.53676601C>T | GRCh37 |
| NC_000001.9:g.53449189C>T | NCBI36 |
| NG_008035.1:g.19501C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371486.4:c.1255C>T MANE Select | ENSP00000360541.3:p.Leu419= | |
| ENST00000635862.1:c.1255C>T | ENSP00000490867.1:p.Leu419= | |
| ENST00000635888.1:c.*1241C>T | ENSP00000490042.1:n.*1241C>T | |
| ENST00000636239.1:c.*902C>T | ENSP00000490066.1:n.*902C>T | |
| ENST00000636867.1:c.1255C>T | ENSP00000489631.1:p.Leu419= | |
| ENST00000636891.1:c.1255C>T | ENSP00000490399.1:p.Leu419= | |
| ENST00000636935.1:c.341-2335C>T | ENSP00000489757.1:n.341-2335C>T | |
| ENST00000637252.1:c.1255C>T | ENSP00000490492.1:p.Leu419= | |
| ENST00000637726.1:n.3455C>T | ||
| ENST00000638135.1:c.*902C>T | ENSP00000489756.1:n.*902C>T | |
| ENST00000371486.3:c.1255C>T | ENSP00000360541.3:p.Leu419= | |
| NM_000098.2:c.1255C>T | NP_000089.1:p.Leu419= | |
| XM_005270484.1:c.1255C>T | XP_005270541.1:p.Leu419= | |
| NM_001330589.1:c.1255C>T | NP_001317518.1:p.Leu419= | |
| NM_000098.3:c.1255C>T MANE Select | NP_000089.1:p.Leu419= | |
| NM_001330589.2:c.1255C>T | NP_001317518.1:p.Leu419= |