HGVS | Genome Assembly |
---|---|
NC_000002.12:g.189008429G= , CM000664.2:g.189008429G= | GRCh38 |
NC_000002.11:g.189873155G= , CM000664.1:g.189873155G= | GRCh37 |
NC_000002.10:g.189581400G= | NCBI36 |
NG_007404.1:g.39057G= , LRG_3:g.39057G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000450867.2:c.3426+287G= | ENSP00000415346.2:n.3426+287G= | |
ENST00000304636.9:c.3525+287G= MANE Select | ENSP00000304408.4:n.3525+287G= | |
ENST00000304636.7:c.3525+287G= | ENSP00000304408.3:n.3525+287G= | |
ENST00000317840.9:c.2616+287G= | ENSP00000315243.6:n.2616+287G= | |
ENST00000487010.1:n.128G= | ||
NM_000090.3:c.3525+287G= , LRG_3t1:c.3525+287G= | NP_000081.1:n.3525+287G= | |
NM_000090.4:c.3525+287G= MANE Select | NP_000081.2:n.3525+287G= |