HGVS | Genome Assembly |
---|---|
NC_000019.10:g.47004083G= , CM000681.2:g.47004083G= | GRCh38 |
NC_000019.9:g.47507340G= , CM000681.1:g.47507340G= | GRCh37 |
NC_000019.8:g.52199180G= | NCBI36 |
NG_047014.1:g.90517G= | |
NG_047014.2:g.148087G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000404338.8:c.7895G= | ENSP00000385720.2:n.7895G= | |
ENST00000672722.1:c.*3395G= MANE Select | ENSP00000500409.1:n.*3395G= | |
ENST00000404338.7:c.7895G= | ENSP00000385720.2:n.7895G= | |
ENST00000614079.1:c.7472G= | ENSP00000483730.1:n.7472G= | |
NM_004491.4:c.7895G= | NP_004482.4:n.7895G= | |
NM_004491.5:c.*3395G= MANE Select | NP_004482.4:n.*3395G= |