Linked Data
MyVariant Identifiers:
chr17:g.45363728A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.47286362A>T , CM000679.2:g.47286362A>T | GRCh38 |
| NC_000017.10:g.45363728A>T , CM000679.1:g.45363728A>T | GRCh37 |
| NC_000017.9:g.42718727A>T | NCBI36 |
| NG_008332.2:g.37521A>T , LRG_481:g.37521A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696963.1:c.717A>T | ENSP00000513002.1:p.Ser239= | |
| ENST00000559488.7:c.717A>T MANE Select | ENSP00000452786.2:p.Ser239= | |
| ENST00000559488.5:c.717A>T | ENSP00000452786.1:p.Ser239= | |
| ENST00000560629.1:c.682A>T | ||
| ENST00000571680.1:c.717A>T | ENSP00000461626.1:p.Ser239= | |
| NM_000212.2:c.717A>T , LRG_481t1:c.717A>T | NP_000203.2:p.Ser239= | |
| NM_000212.3:c.717A>T MANE Select | NP_000203.2:p.Ser239= |