Linked Data
MyVariant Identifiers:
chr17:g.7978914T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8075596T>A , CM000679.2:g.8075596T>A | GRCh38 |
| NC_000017.10:g.7978914T>A , CM000679.1:g.7978914T>A | GRCh37 |
| NC_000017.9:g.7919639T>A | NCBI36 |
| NG_007099.1:g.17108A>T | |
| NG_007099.2:g.17121A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000647874.1:c.1653A>T MANE Select | ENSP00000497784.1:p.Ser551= | |
| ENST00000649809.1:c.717A>T | ENSP00000496845.1:p.Ser239= | |
| ENST00000319144.4:c.1653A>T | ENSP00000315167.4:p.Ser551= | |
| ENST00000577351.5:n.479+579A>T | ||
| NM_001139.2:c.1653A>T | NP_001130.1:p.Ser551= | |
| NM_001139.3:c.1653A>T MANE Select | NP_001130.1:p.Ser551= |