HGVS | Genome Assembly |
---|---|
NC_000020.11:g.23047791G= , CM000682.2:g.23047791G= | GRCh38 |
NC_000020.10:g.23028428G= , CM000682.1:g.23028428G= | GRCh37 |
NC_000020.9:g.22976428G= | NCBI36 |
NG_012027.1:g.6874C= , LRG_168:g.6874C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000377103.3:c.1714C= MANE Select | ENSP00000366307.2:p.Pro572= | |
ENST00000377103.2:c.1714C= | ENSP00000366307.2:p.Pro572= | |
NM_000361.2:c.1714C= , LRG_168t1:c.1714C= | NP_000352.1:p.Pro572= | |
NM_000361.3:c.1714C= MANE Select | NP_000352.1:p.Pro572= |