Linked Data
MyVariant Identifiers:
chr1:g.186099180C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186130048C>G , CM000663.2:g.186130048C>G | GRCh38 |
| NC_000001.10:g.186099180C>G , CM000663.1:g.186099180C>G | GRCh37 |
| NC_000001.9:g.184365803C>G | NCBI36 |
| NG_011841.1:g.400498C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000271588.9:c.12987C>G MANE Select | ENSP00000271588.4:p.Thr4329= | |
| ENST00000271588.8:c.12987C>G | ENSP00000271588.4:p.Thr4329= | |
| NM_031935.2:c.12987C>G | NP_114141.2:p.Thr4329= | |
| XM_011510037.1:c.12702C>G | XP_011508339.1:p.Thr4234= | |
| XM_011510038.1:c.12987C>G | XP_011508340.1:p.Thr4329= | |
| XM_011510039.1:c.12987C>G | XP_011508341.1:p.Thr4329= | |
| XM_011510038.3:c.12987C>G | XP_011508340.1:p.Thr4329= | |
| XM_017002437.1:c.11010C>G | XP_016857926.1:p.Thr3670= | |
| NM_031935.3:c.12987C>G MANE Select | NP_114141.2:p.Thr4329= |