Linked Data
MyVariant Identifiers:
chr1:g.12025587C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.11965530C>G , CM000663.2:g.11965530C>G | GRCh38 |
| NC_000001.10:g.12025587C>G , CM000663.1:g.12025587C>G | GRCh37 |
| NC_000001.9:g.11948174C>G | NCBI36 |
| NG_008159.1:g.35842C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000196061.5:c.1521C>G MANE Select | ENSP00000196061.4:p.Ser507= | |
| ENST00000196061.4:c.1521C>G | ENSP00000196061.4:p.Ser507= | |
| ENST00000470133.1:n.135C>G | ||
| ENST00000491536.5:n.149C>G | ||
| NM_000302.3:c.1521C>G | NP_000293.2:p.Ser507= | |
| NM_001316320.1:c.1662C>G | NP_001303249.1:p.Ser554= | |
| XM_011541594.1:c.1602C>G | XP_011539896.1:p.Ser534= | |
| XM_024447707.1:c.855C>G | XP_024303475.1:p.Ser285= | |
| NM_000302.4:c.1521C>G MANE Select | NP_000293.2:p.Ser507= | |
| NM_001316320.2:c.1662C>G | NP_001303249.1:p.Ser554= |