HGVS | Genome Assembly |
---|---|
NC_000019.10:g.47004270G= , CM000681.2:g.47004270G= | GRCh38 |
NC_000019.9:g.47507527G= , CM000681.1:g.47507527G= | GRCh37 |
NC_000019.8:g.52199367G= | NCBI36 |
NG_047014.1:g.90704G= | |
NG_047014.2:g.148274G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000404338.8:c.8082G= | ENSP00000385720.2:n.8082G= | |
ENST00000672722.1:c.*3582G= MANE Select | ENSP00000500409.1:n.*3582G= | |
ENST00000404338.7:c.8082G= | ENSP00000385720.2:n.8082G= | |
ENST00000614079.1:c.7659G= | ENSP00000483730.1:n.7659G= | |
NM_004491.4:c.8082G= | NP_004482.4:n.8082G= | |
NM_004491.5:c.*3582G= MANE Select | NP_004482.4:n.*3582G= |