HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1433390G= , CM000667.2:g.1433390G= | GRCh38 |
NC_000005.9:g.1433505G= , CM000667.1:g.1433505G= | GRCh37 |
NC_000005.8:g.1486505G= | NCBI36 |
NG_015885.1:g.17039C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270349.12:c.419-692C= MANE Select | ENSP00000270349.9:n.419-692C= | |
ENST00000270349.11:c.419-692C= | ENSP00000270349.9:n.419-692C= | |
NM_001044.4:c.419-692C= | NP_001035.1:n.419-692C= | |
NM_001044.5:c.419-692C= MANE Select | NP_001035.1:n.419-692C= |