Linked Data
MyVariant Identifiers:
chr2:g.233388570C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.232523860C>G , CM000664.2:g.232523860C>G | GRCh38 |
| NC_000002.11:g.233388570C>G , CM000664.1:g.233388570C>G | GRCh37 |
| NC_000002.10:g.233096814C>G | NCBI36 |
| NG_008028.1:g.2649C>G | |
| NG_031969.1:g.8398C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000617714.2:c.1101C>G MANE Select | ENSP00000479745.1:p.Ala367= | |
| ENST00000449534.6:c.1104C>G | ENSP00000473410.1:p.Ala368= | |
| ENST00000617714.1:c.1101C>G | ENSP00000479745.1:p.Ala367= | |
| NM_001195129.1:c.1101C>G | NP_001182058.1:p.Ala367= | |
| NM_001195129.2:c.1101C>G MANE Select | NP_001182058.1:p.Ala367= | |
| NM_001369848.1:c.1104C>G | NP_001356777.1:p.Ala368= |