HGVS | Genome Assembly |
---|---|
NC_000005.10:g.177992717A>T , CM000667.2:g.177992717A>T | GRCh38 |
NC_000005.9:g.177419718A>T , CM000667.1:g.177419718A>T | GRCh37 |
NC_000005.8:g.177352324A>T | NCBI36 |
NG_015889.1:g.8526T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000308304.2:c.673T>A MANE Select | ENSP00000311290.2:p.Trp225Arg | |
NM_006261.4:c.673T>A | NP_006252.3:p.Trp225Arg | |
NM_006261.5:c.673T>A MANE Select | NP_006252.4:p.Trp225Arg |