Linked Data
MyVariant Identifiers:
chr17:g.7979028C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8075710C>A , CM000679.2:g.8075710C>A | GRCh38 |
| NC_000017.10:g.7979028C>A , CM000679.1:g.7979028C>A | GRCh37 |
| NC_000017.9:g.7919753C>A | NCBI36 |
| NG_007099.1:g.16994G>T | |
| NG_007099.2:g.17007G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647874.1:c.1539G>T MANE Select | ENSP00000497784.1:p.Val513= | |
| ENST00000649809.1:c.603G>T | ENSP00000496845.1:p.Val201= | |
| ENST00000319144.4:c.1539G>T | ENSP00000315167.4:p.Val513= | |
| ENST00000577351.5:n.479+465G>T | ||
| NM_001139.2:c.1539G>T | NP_001130.1:p.Val513= | |
| NM_001139.3:c.1539G>T MANE Select | NP_001130.1:p.Val513= |