Linked Data
MyVariant Identifiers:
chr18:g.29121214C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31541251C>G , CM000680.2:g.31541251C>G | GRCh38 |
| NC_000018.9:g.29121214C>G , CM000680.1:g.29121214C>G | GRCh37 |
| NC_000018.8:g.27375212C>G | NCBI36 |
| NG_007072.3:g.48010C>G , LRG_397:g.48010C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261590.13:c.1938C>G MANE Select | ENSP00000261590.8:p.Pro646= | |
| ENST00000261590.12:c.1938C>G | ENSP00000261590.8:p.Pro646= | |
| NM_001943.3:c.1938C>G , LRG_397t1:c.1938C>G | NP_001934.2:p.Pro646= | |
| NM_001943.4:c.1938C>G | NP_001934.2:p.Pro646= | |
| XM_024451095.1:c.1404C>G | XP_024306863.1:p.Pro468= | |
| NM_001943.5:c.1938C>G MANE Select | NP_001934.2:p.Pro646= |