HGVS | Genome Assembly |
---|---|
NC_000016.10:g.88738280G>T , CM000678.2:g.88738280G>T | GRCh38 |
NC_000016.9:g.88804688G>T , CM000678.1:g.88804688G>T | GRCh37 |
NC_000016.8:g.87332189G>T | NCBI36 |
NG_042229.1:g.51941C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000301015.14:c.795C>A (PIEZO1) MANE Select | ENSP00000301015.9:p.Cys265Ter | |
ENST00000301015.13:c.795C>A (PIEZO1) | ENSP00000301015.9:p.Cys265Ter | |
NM_001142864.2:c.795C>A (PIEZO1) | NP_001136336.2:p.Cys265Ter | |
NM_001142864.3:c.795C>A (PIEZO1) | NP_001136336.2:p.Cys265Ter | |
NR_103774.1:n.729G>T (HSALR1) | ||
NM_001142864.4:c.795C>A (PIEZO1) MANE Select | NP_001136336.2:p.Cys265Ter |