Linked Data
MyVariant Identifiers:
chr1:g.94497364G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94031808G>C , CM000663.2:g.94031808G>C | GRCh38 |
| NC_000001.10:g.94497364G>C , CM000663.1:g.94497364G>C | GRCh37 |
| NC_000001.9:g.94269952G>C | NCBI36 |
| NG_009073.1:g.94342C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.4098C>G MANE Select | ENSP00000359245.3:p.Thr1366= | |
| ENST00000370225.3:c.4098C>G | ENSP00000359245.3:p.Thr1366= | |
| ENST00000536513.5:c.474C>G | ENSP00000439707.2:p.Thr158= | |
| NM_000350.2:c.4098C>G | NP_000341.2:p.Thr1366= | |
| NM_000350.3:c.4098C>G MANE Select | NP_000341.2:p.Thr1366= |