Linked Data
MyVariant Identifiers:
chr17:g.62019109C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.63941749C>A , CM000679.2:g.63941749C>A | GRCh38 |
| NC_000017.10:g.62019109C>A , CM000679.1:g.62019109C>A | GRCh37 |
| NC_000017.9:g.59372841C>A | NCBI36 |
| NG_011699.1:g.36170G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000435607.3:c.4533G>T MANE Select | ENSP00000396320.1:p.Ser1511= | |
| ENST00000578147.5:c.4533G>T | ENSP00000463963.1:p.Ser1511= | |
| NM_000334.4:c.4533G>T MANE Select | NP_000325.4:p.Ser1511= | |
| XM_005257566.3:c.4533G>T | XP_005257623.1:p.Ser1511= |