HGVS | Genome Assembly |
---|---|
NC_000007.14:g.152648833C= , CM000669.2:g.152648833C= | GRCh38 |
NC_000007.13:g.152345918C= , CM000669.1:g.152345918C= | GRCh37 |
NC_000007.12:g.151976851C= | NCBI36 |
NG_027988.1:g.32333G= | |
NG_027988.2:g.32333G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000698506.1:c.484G= | ENSP00000513758.1:p.Asp162= | |
ENST00000359321.2:c.652G= MANE Select | ENSP00000352271.1:p.Asp218= | |
ENST00000359321.1:c.652G= | ENSP00000352271.1:p.Asp218= | |
ENST00000495707.1:n.674G= | ||
NM_005431.1:c.652G= | NP_005422.1:p.Asp218= | |
NM_005431.2:c.652G= MANE Select | NP_005422.1:p.Asp218= |