HGVS | Genome Assembly |
---|---|
NC_000011.10:g.2445336G= , CM000673.2:g.2445336G= | GRCh38 |
NC_000011.9:g.2466566G= , CM000673.1:g.2466566G= | GRCh37 |
NC_000011.8:g.2423142G= | NCBI36 |
NG_008935.1:g.5346G= , LRG_287:g.5346G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000496887.7:c.24-47G= | ENSP00000434560.2:n.24-47G= | |
ENST00000646564.2:c.238G= | ENSP00000495806.2:p.Gly80= | |
ENST00000155840.12:c.238G= MANE Select | ENSP00000155840.2:p.Gly80= | |
ENST00000155840.9:c.238G= | ENSP00000155840.2:p.Gly80= | |
ENST00000345015.4:n.15G= | ||
ENST00000496887.6:c.24-47G= | ENSP00000434560.1:n.24-47G= | |
NM_000218.2:c.238G= , LRG_287t1:c.238G= | NP_000209.2:p.Gly80= | |
NM_000218.3:c.238G= MANE Select | NP_000209.2:p.Gly80= |