Linked Data
MyVariant Identifiers:
chr12:g.58157511G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57763728G>C , CM000674.2:g.57763728G>C | GRCh38 |
| NC_000012.11:g.58157511G>C , CM000674.1:g.58157511G>C | GRCh37 |
| NC_000012.10:g.56443778G>C | NCBI36 |
| NG_007076.1:g.8466C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000713544.1:c.1377C>G | ENSP00000518840.1:p.Arg459= | |
| ENST00000713545.1:c.*301C>G | ENSP00000518841.1:n.*301C>G | |
| ENST00000228606.9:c.1296C>G MANE Select | ENSP00000228606.4:p.Arg432= | |
| ENST00000228606.8:c.1296C>G | ENSP00000228606.4:p.Arg432= | |
| ENST00000547344.5:n.1435C>G | ||
| NM_000785.3:c.1296C>G | NP_000776.1:p.Arg432= | |
| NM_000785.4:c.1296C>G MANE Select | NP_000776.1:p.Arg432= |