HGVS | Genome Assembly |
---|---|
NC_000001.11:g.115732972A>C , CM000663.2:g.115732972A>C | GRCh38 |
NC_000001.10:g.116275593A>C , CM000663.1:g.116275593A>C | GRCh37 |
NC_000001.9:g.116077116A>C | NCBI36 |
NG_008802.1:g.40834T>G , LRG_404:g.40834T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000488931.2:c.259T>G | ENSP00000518226.1:p.Tyr87Asp | |
ENST00000261448.6:c.535T>G MANE Select | ENSP00000261448.5:p.Tyr179Asp | |
ENST00000261448.5:c.535T>G | ENSP00000261448.5:p.Tyr179Asp | |
NM_001232.3:c.535T>G , LRG_404t1:c.535T>G | NP_001223.2:p.Tyr179Asp | |
NM_001232.4:c.535T>G MANE Select | NP_001223.2:p.Tyr179Asp |