Linked Data
MyVariant Identifiers:
chr1:g.147380349C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.147908222C>G , CM000663.2:g.147908222C>G | GRCh38 |
| NC_000001.10:g.147380349C>G , CM000663.1:g.147380349C>G | GRCh37 |
| NC_000001.9:g.145846973C>G | NCBI36 |
| NG_016242.1:g.10404C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369235.2:c.267C>G MANE Select | ENSP00000358238.1:p.Ser89= | |
| ENST00000369235.1:c.267C>G | ENSP00000358238.1:p.Ser89= | |
| NM_005267.4:c.267C>G | NP_005258.2:p.Ser89= | |
| XM_011509416.1:c.267C>G | XP_011507718.1:p.Ser89= | |
| XM_011509417.1:c.267C>G | XP_011507719.1:p.Ser89= | |
| XM_011509417.2:c.267C>G | XP_011507719.1:p.Ser89= | |
| XR_002956281.1:n.1182C>G | ||
| NM_005267.5:c.267C>G MANE Select | NP_005258.2:p.Ser89= |