HGVS | Genome Assembly |
---|---|
NC_000007.14:g.152660663A= , CM000669.2:g.152660663A= | GRCh38 |
NC_000007.13:g.152357748A= , CM000669.1:g.152357748A= | GRCh37 |
NC_000007.12:g.151988681A= | NCBI36 |
NG_027988.1:g.20503T= | |
NG_027988.2:g.20503T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000698506.1:c.-47-11300T= | ENSP00000513758.1:n.-47-11300T= | |
ENST00000698507.1:n.227T= | ||
ENST00000359321.2:c.121+38T= MANE Select | ENSP00000352271.1:n.121+38T= | |
ENST00000359321.1:c.121+38T= | ENSP00000352271.1:n.121+38T= | |
ENST00000495707.1:n.143+38T= | ||
NM_005431.1:c.121+38T= | NP_005422.1:n.121+38T= | |
NM_005431.2:c.121+38T= MANE Select | NP_005422.1:n.121+38T= |