Linked Data
MyVariant Identifiers:
chr1:g.159856369T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.159886579T>C , CM000663.2:g.159886579T>C | GRCh38 |
| NC_000001.10:g.159856369T>C , CM000663.1:g.159856369T>C | GRCh37 |
| NC_000001.9:g.158122993T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368099.9:c.699A>G MANE Select | ENSP00000357079.4:p.Glu233= | |
| ENST00000368099.8:c.699A>G | ENSP00000357079.4:p.Glu233= | |
| ENST00000426543.6:c.444A>G | ENSP00000403044.2:p.Glu148= | |
| ENST00000476696.5:c.699A>G | ENSP00000483972.1:p.Glu233= | |
| NM_012337.2:c.699A>G | NP_036469.2:p.Glu233= | |
| NM_012337.3:c.699A>G MANE Select | NP_036469.2:p.Glu233= |