Linked Data
MyVariant Identifiers:
chr9:g.101983916G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.99221634G>C , CM000671.2:g.99221634G>C | GRCh38 |
| NC_000009.11:g.101983916G>C , CM000671.1:g.101983916G>C | GRCh37 |
| NC_000009.10:g.101023737G>C | NCBI36 |
| NG_008928.1:g.5331C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000476832.2:c.261C>G MANE Select | ENSP00000417764.1:p.Ala87= | |
| ENST00000238477.5:c.261C>G | ENSP00000432675.2:p.Ala87= | |
| ENST00000476832.1:c.261C>G | ENSP00000417764.1:p.Ala87= | |
| NM_033087.3:c.261C>G | NP_149078.1:p.Ala87= | |
| NR_024532.1:n.331C>G | ||
| NM_033087.4:c.261C>G MANE Select | NP_149078.1:p.Ala87= | |
| NR_024532.2:n.309C>G |