Linked Data
gnomAD v4:
3-129532292-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.129532292A>T , CM000665.2:g.129532292A>T | GRCh38 |
| NC_000003.11:g.129251135A>T , CM000665.1:g.129251135A>T | GRCh37 |
| NC_000003.10:g.130733825A>T | NCBI36 |
| NG_009115.1:g.8654A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000296271.4:c.572A>T MANE Select | ENSP00000296271.3:p.Tyr191Phe | |
| ENST00000296271.3:c.572A>T | ENSP00000296271.3:p.Tyr191Phe | |
| NM_000539.3:c.572A>T MANE Select | NP_000530.1:p.Tyr191Phe |