Linked Data
gnomAD v4:
10-123034461-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.123034461C>T , CM000672.2:g.123034461C>T | GRCh38 |
| NC_000010.10:g.124793977C>T , CM000672.1:g.124793977C>T | GRCh37 |
| NC_000010.9:g.124783967C>T | NCBI36 |
| NG_008003.1:g.30549C>T , LRG_451:g.30549C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000358776.7:c.148C>T MANE Select | ENSP00000357873.3:p.His50Tyr | |
| ENST00000358776.6:c.148C>T | ENSP00000357873.3:p.His50Tyr | |
| ENST00000368869.8:c.-58C>T | ENSP00000357862.4:n.-58C>T | |
| ENST00000411816.2:n.165C>T | ||
| NM_001609.3:c.148C>T , LRG_451t1:c.148C>T | NP_001600.1:p.His50Tyr | |
| NM_001330174.1:c.-58C>T | NP_001317103.1:n.-58C>T | |
| NM_001330174.2:c.-58C>T | NP_001317103.1:n.-58C>T | |
| NM_001609.4:c.148C>T MANE Select | NP_001600.1:p.His50Tyr | |
| NM_001330174.3:c.-58C>T | NP_001317103.1:n.-58C>T |