HGVS | Genome Assembly |
---|---|
NC_000005.10:g.136046203T= , CM000667.2:g.136046203T= | GRCh38 |
NC_000005.9:g.135381892T= , CM000667.1:g.135381892T= | GRCh37 |
NC_000005.8:g.135409791T= | NCBI36 |
NG_012646.1:g.22309T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000442011.7:c.299-132T= MANE Select | ENSP00000416330.2:n.299-132T= | |
ENST00000442011.6:c.299-132T= | ENSP00000416330.2:n.299-132T= | |
ENST00000504185.5:n.456-132T= | ||
ENST00000506699.5:n.364-132T= | ||
ENST00000507018.5:c.216-132T= | ||
ENST00000515433.1:n.459T= | ||
NM_000358.2:c.299-132T= | NP_000349.1:n.299-132T= | |
NM_000358.3:c.299-132T= MANE Select | NP_000349.1:n.299-132T= |