Linked Data
MyVariant Identifiers:
chr1:g.168262459A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.168293221A>T , CM000663.2:g.168293221A>T | GRCh38 |
| NC_000001.10:g.168262459A>T , CM000663.1:g.168262459A>T | GRCh37 |
| NC_000001.9:g.166529083A>T | NCBI36 |
| NG_008244.1:g.17182A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000367821.8:c.546A>T MANE Select | ENSP00000356795.3:p.Thr182= | |
| ENST00000367821.7:c.546A>T | ENSP00000356795.3:p.Thr182= | |
| ENST00000431969.5:c.343A>T | ||
| NM_005149.2:c.546A>T | NP_005140.1:p.Thr182= | |
| NM_005149.3:c.546A>T MANE Select | NP_005140.1:p.Thr182= |