HGVS | Genome Assembly |
---|---|
NC_000023.11:g.153688894A= , CM000685.2:g.153688894A= | GRCh38 |
NC_000023.10:g.152954349A= , CM000685.1:g.152954349A= | GRCh37 |
NC_000023.9:g.152607543A= | NCBI36 |
NG_012016.1:g.5598A= | |
NG_012016.2:g.5598A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000253122.10:c.262+58A= (SLC6A8) MANE Select | ENSP00000253122.5:n.262+58A= | |
ENST00000253122.9:c.262+58A= (SLC6A8) | ENSP00000253122.5:n.262+58A= | |
ENST00000458354.5:c.-82T= (PNCK) | ENSP00000401542.1:n.-82T= | |
ENST00000476466.1:n.114+58A= (SLC6A8) | ||
NM_001142805.1:c.262+58A= (SLC6A8) | NP_001136277.1:n.262+58A= | |
NM_005629.3:c.262+58A= (SLC6A8) | NP_005620.1:n.262+58A= | |
NM_005629.4:c.262+58A= (SLC6A8) MANE Select | NP_005620.1:n.262+58A= | |
NM_001142805.2:c.262+58A= (SLC6A8) | NP_001136277.1:n.262+58A= |