HGVS | Genome Assembly |
---|---|
NC_000017.11:g.10409163A>C , CM000679.2:g.10409163A>C | GRCh38 |
NC_000017.10:g.10312480A>C , CM000679.1:g.10312480A>C | GRCh37 |
NC_000017.9:g.10253205A>C | NCBI36 |
NG_013015.1:g.17788T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000403437.2:c.1899T>G (MYH8) MANE Select | ENSP00000384330.2:p.Asp633Glu | |
NM_002472.2:c.1899T>G (MYH8) | NP_002463.2:p.Asp633Glu | |
NR_125367.1:n.167+2925A>C (MYHAS) | ||
XM_011523873.1:c.1899T>G (MYH8) | XP_011522175.1:p.Asp633Glu | |
XM_011523874.1:c.1899T>G (MYH8) | XP_011522176.1:p.Asp633Glu | |
NM_002472.3:c.1899T>G (MYH8) MANE Select | NP_002463.2:p.Asp633Glu |