Linked Data
MyVariant Identifiers:
chr2:g.113590294A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.112832717A>C , CM000664.2:g.112832717A>C | GRCh38 |
| NC_000002.11:g.113590294A>C , CM000664.1:g.113590294A>C | GRCh37 |
| NC_000002.10:g.113306765A>C | NCBI36 |
| NG_008851.1:g.9063T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000263341.7:c.411T>G MANE Select | ENSP00000263341.2:p.Ser137= | |
| ENST00000263341.6:c.411T>G | ENSP00000263341.2:p.Ser137= | |
| ENST00000418817.5:c.411T>G | ENSP00000407219.1:p.Ser137= | |
| ENST00000487639.1:n.312T>G | ||
| ENST00000491056.5:n.1218T>G | ||
| NM_000576.2:c.411T>G | NP_000567.1:p.Ser137= | |
| XM_006712496.1:c.177T>G | XP_006712559.1:p.Ser59= | |
| XM_017003988.2:c.318T>G | XP_016859477.1:p.Ser106= | |
| NM_000576.3:c.411T>G MANE Select | NP_000567.1:p.Ser137= |