Linked Data
MyVariant Identifiers:
chr17:g.28548665G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.30221647G>C , CM000679.2:g.30221647G>C | GRCh38 |
| NC_000017.10:g.28548665G>C , CM000679.1:g.28548665G>C | GRCh37 |
| NC_000017.9:g.25572791G>C | NCBI36 |
| NG_011747.2:g.19290C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650711.1:c.312C>G MANE Select | ENSP00000498537.1:p.Arg104= | |
| ENST00000261707.7:c.312C>G | ENSP00000261707.3:p.Arg104= | |
| ENST00000394821.2:c.312C>G | ENSP00000378298.2:p.Arg104= | |
| ENST00000401766.6:c.312C>G | ENSP00000385822.2:p.Arg104= | |
| NM_001045.5:c.312C>G | NP_001036.1:p.Arg104= | |
| NM_001045.6:c.312C>G MANE Select | NP_001036.1:p.Arg104= |