Linked Data
MyVariant Identifiers:
chr17:g.39740141T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41583889T>G , CM000679.2:g.41583889T>G | GRCh38 |
| NC_000017.10:g.39740141T>G , CM000679.1:g.39740141T>G | GRCh37 |
| NC_000017.9:g.36993667T>G | NCBI36 |
| NG_008624.1:g.8007A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.798A>C MANE Select | ENSP00000167586.6:p.Gly266= | |
| ENST00000167586.6:c.798A>C | ENSP00000167586.6:p.Gly266= | |
| ENST00000476662.1:n.248A>C | ||
| NM_000526.4:c.798A>C | NP_000517.2:p.Gly266= | |
| NM_000526.5:c.798A>C MANE Select | NP_000517.3:p.Gly266= |