Linked Data
MyVariant Identifiers:
chr2:g.27308113C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.27085245C>G , CM000664.2:g.27085245C>G | GRCh38 |
| NC_000002.11:g.27308113C>G , CM000664.1:g.27308113C>G | GRCh37 |
| NC_000002.10:g.27161617C>G | NCBI36 |
| NG_012199.1:g.3503C>G | |
| NG_046849.1:g.11679C>G | |
| NG_012199.2:g.3503C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000380320.9:c.2661C>G MANE Select | ENSP00000369677.4:p.Val887= | |
| ENST00000380320.8:c.2661C>G | ENSP00000369677.4:p.Val887= | |
| ENST00000433140.1:c.653C>G | ||
| NM_007046.3:c.2661C>G | NP_008977.1:p.Val887= | |
| XM_006711928.2:c.2575+237C>G | XP_006711991.1:n.2575+237C>G | |
| NM_007046.4:c.2661C>G MANE Select | NP_008977.1:p.Val887= |