HGVS | Genome Assembly |
---|---|
NC_000012.12:g.65170074A>T , CM000674.2:g.65170074A>T | GRCh38 |
NC_000012.11:g.65563854A>T , CM000674.1:g.65563854A>T | GRCh37 |
NC_000012.10:g.63850121A>T | NCBI36 |
NG_016210.1:g.5504A>T | |
NG_016210.2:g.5504A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000308330.3:c.478A>T MANE Select | ENSP00000308369.2:p.Lys160Ter | |
ENST00000308330.2:c.478A>T | ENSP00000308369.2:p.Lys160Ter | |
ENST00000541171.1:n.492A>T | ||
NM_001167614.1:c.478A>T | NP_001161086.1:p.Lys160Ter | |
NM_014319.4:c.478A>T | NP_055134.2:p.Lys160Ter | |
NM_014319.5:c.478A>T MANE Select | NP_055134.2:p.Lys160Ter | |
NM_001167614.2:c.478A>T | NP_001161086.1:p.Lys160Ter |