Linked Data
MyVariant Identifiers:
chr4:g.120241966A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.119320811A>T , CM000666.2:g.119320811A>T | GRCh38 |
| NC_000004.11:g.120241966A>T , CM000666.1:g.120241966A>T | GRCh37 |
| NC_000004.10:g.120461414A>T | NCBI36 |
| NG_011444.1:g.6351T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000274024.4:c.99T>A MANE Select | ENSP00000274024.3:p.Ala33= | |
| ENST00000274024.3:c.99T>A | ENSP00000274024.3:p.Ala33= | |
| NM_000134.3:c.99T>A | NP_000125.2:p.Ala33= | |
| NM_000134.4:c.99T>A MANE Select | NP_000125.2:p.Ala33= |