HGVS | Genome Assembly |
---|---|
NC_000022.11:g.37576525C= , CM000684.2:g.37576525C= | GRCh38 |
NC_000022.10:g.37972532C= , CM000684.1:g.37972532C= | GRCh37 |
NC_000022.9:g.36302478C= | NCBI36 |
NG_012096.1:g.8493G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000215886.6:c.6+3375G= MANE Select | ENSP00000215886.4:n.6+3375G= | |
ENST00000215886.5:c.6+3375G= | ENSP00000215886.4:n.6+3375G= | |
ENST00000416480.1:c.6+3375G= | ENSP00000407351.1:n.6+3375G= | |
NM_006498.2:c.6+3375G= | NP_006489.1:n.6+3375G= | |
NM_006498.3:c.6+3375G= MANE Select | NP_006489.1:n.6+3375G= |