gnomAD v2:
ClinVar RCV:
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.7568443C>T , CM000668.2:g.7568443C>T | GRCh38 |
| NC_000006.11:g.7568676C>T , CM000668.1:g.7568676C>T | GRCh37 |
| NC_000006.10:g.7513675C>T | NCBI36 |
| NG_008803.1:g.31807C>T , LRG_423:g.31807C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000710359.1:c.1273C>T | ENSP00000518230.1:p.Arg425Ter | |
| ENST00000682228.1:n.1458C>T | ||
| ENST00000379802.8:c.1273C>T MANE Select | ENSP00000369129.3:p.Arg425Ter | |
| ENST00000379802.7:c.1273C>T | ENSP00000369129.3:p.Arg425Ter | |
| ENST00000418664.2:c.1273C>T | ENSP00000396591.2:p.Arg425Ter | |
| NM_001008844.1:c.1273C>T | NP_001008844.1:p.Arg425Ter | |
| NM_004415.2:c.1273C>T , LRG_423t1:c.1273C>T | NP_004406.2:p.Arg425Ter | |
| XM_011514323.1:c.1273C>T | XP_011512625.1:p.Arg425Ter | |
| NM_001008844.2:c.1273C>T | NP_001008844.1:p.Arg425Ter | |
| NM_001319034.1:c.1273C>T | NP_001305963.1:p.Arg425Ter | |
| NM_004415.3:c.1273C>T | NP_004406.2:p.Arg425Ter | |
| NM_004415.4:c.1273C>T MANE Select | NP_004406.2:p.Arg425Ter | |
| NM_001008844.3:c.1273C>T | NP_001008844.1:p.Arg425Ter | |
| NM_001319034.2:c.1273C>T | NP_001305963.1:p.Arg425Ter |