Linked Data
MyVariant Identifiers:
chr12:g.122295309G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.121857403G>C , CM000674.2:g.121857403G>C | GRCh38 |
| NC_000012.11:g.122295309G>C , CM000674.1:g.122295309G>C | GRCh37 |
| NC_000012.10:g.120779692G>C | NCBI36 |
| NG_016461.1:g.36209C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000289004.8:c.123C>G (HPD) MANE Select | ENSP00000289004.4:p.Gly41= | |
| ENST00000535114.1:n.479C>G (HPD) | ||
| ENST00000542159.2:n.181C>G (HPD) | ||
| ENST00000543163.5:c.6C>G (HPD) | ENSP00000441677.1:p.Gly2= | |
| NM_001171993.1:c.6C>G (HPD) | NP_001165464.1:p.Gly2= | |
| NM_002150.2:c.123C>G (HPD) | NP_002141.1:p.Gly41= | |
| XR_002957437.1:n.324-216G>C (TIALD) | ||
| NM_002150.3:c.123C>G (HPD) MANE Select | NP_002141.2:p.Gly41= | |
| NM_001171993.2:c.6C>G (HPD) | NP_001165464.1:p.Gly2= |