Linked Data
MyVariant Identifiers:
chr17:g.7979025C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8075707C>A , CM000679.2:g.8075707C>A | GRCh38 |
| NC_000017.10:g.7979025C>A , CM000679.1:g.7979025C>A | GRCh37 |
| NC_000017.9:g.7919750C>A | NCBI36 |
| NG_007099.1:g.16997G>T | |
| NG_007099.2:g.17010G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647874.1:c.1542G>T MANE Select | ENSP00000497784.1:p.Thr514= | |
| ENST00000649809.1:c.606G>T | ENSP00000496845.1:p.Thr202= | |
| ENST00000319144.4:c.1542G>T | ENSP00000315167.4:p.Thr514= | |
| ENST00000577351.5:n.479+468G>T | ||
| NM_001139.2:c.1542G>T | NP_001130.1:p.Thr514= | |
| NM_001139.3:c.1542G>T MANE Select | NP_001130.1:p.Thr514= |