Linked Data
MyVariant Identifiers:
chr12:g.115112387C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.114674582C>G , CM000674.2:g.114674582C>G | GRCh38 |
| NC_000012.11:g.115112387C>G , CM000674.1:g.115112387C>G | GRCh37 |
| NC_000012.10:g.113596770C>G | NCBI36 |
| NG_008315.1:g.14583G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000349155.7:c.1293G>C MANE Select | ENSP00000257567.2:p.Ala431= | |
| ENST00000257566.7:c.1353G>C | ENSP00000257566.3:p.Ala451= | |
| ENST00000349155.6:c.1293G>C | ENSP00000257567.2:p.Ala431= | |
| ENST00000613550.1:c.1293G>C | ENSP00000480048.1:p.Ala431= | |
| NM_005996.3:c.1293G>C | NP_005987.3:p.Ala431= | |
| NM_016569.3:c.1353G>C | NP_057653.3:p.Ala451= | |
| NM_005996.4:c.1293G>C MANE Select | NP_005987.3:p.Ala431= | |
| NM_016569.4:c.1353G>C | NP_057653.3:p.Ala451= |