Linked Data
MyVariant Identifiers:
chr17:g.39023334A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.40867082A>C , CM000679.2:g.40867082A>C | GRCh38 |
| NC_000017.10:g.39023334A>C , CM000679.1:g.39023334A>C | GRCh37 |
| NC_000017.9:g.36276860A>C | NCBI36 |
| NG_008077.1:g.5129T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251643.5:c.105T>G MANE Select | ENSP00000251643.4:p.Ala35= | |
| ENST00000647902.1:c.105T>G | ENSP00000497770.1:p.Ala35= | |
| ENST00000251643.4:c.105T>G | ENSP00000251643.4:p.Ala35= | |
| NM_000223.3:c.105T>G | NP_000214.1:p.Ala35= | |
| XR_934754.1:n.1500+16222A>C | ||
| XR_934754.2:n.2008+16222A>C | ||
| NM_000223.4:c.105T>G MANE Select | NP_000214.1:p.Ala35= |