HGVS | Genome Assembly |
---|---|
NC_000017.11:g.42909383A>C , CM000679.2:g.42909383A>C | GRCh38 |
NC_000017.10:g.41061400A>C , CM000679.1:g.41061400A>C | GRCh37 |
NC_000017.9:g.38314926A>C | NCBI36 |
NG_011808.1:g.13586A>C , LRG_147:g.13586A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000253801.7:c.527A>C MANE Select | ENSP00000253801.1:p.His176Pro | |
ENST00000253801.6:c.527A>C | ENSP00000253801.1:p.His176Pro | |
ENST00000585489.1:c.447-1532A>C | ENSP00000466202.1:n.447-1532A>C | |
ENST00000592383.5:c.450A>C | ENSP00000465958.1:p.Ser150= | |
NM_000151.3:c.527A>C | NP_000142.2:p.His176Pro | |
NM_001270397.1:c.450A>C | NP_001257326.1:p.Ser150= | |
NM_000151.4:c.527A>C MANE Select | NP_000142.2:p.His176Pro | |
NM_001270397.2:c.450A>C | NP_001257326.1:p.Ser150= |