Linked Data
ClinVar Variation Id:
2986362
ClinVar RCV Id:
RCV003844033
MyVariant Identifiers:
chr17:g.62022114G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.63944754G>T , CM000679.2:g.63944754G>T | GRCh38 |
| NC_000017.10:g.62022114G>T , CM000679.1:g.62022114G>T | GRCh37 |
| NC_000017.9:g.59375846G>T | NCBI36 |
| NG_011699.1:g.33165C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000435607.3:c.3831C>A MANE Select | ENSP00000396320.1:p.Ile1277= | |
| ENST00000578147.5:c.3831C>A | ENSP00000463963.1:p.Ile1277= | |
| NM_000334.4:c.3831C>A MANE Select | NP_000325.4:p.Ile1277= | |
| XM_005257566.3:c.3831C>A | XP_005257623.1:p.Ile1277= |