HGVS | Genome Assembly |
---|---|
NC_000001.11:g.149927568A= , CM000663.2:g.149927568A= | GRCh38 |
NC_000001.10:g.149899460A= , CM000663.1:g.149899460A= | GRCh37 |
NC_000001.9:g.148166084A= | NCBI36 |
NG_032777.1:g.5685T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000271628.9:c.34+158T= MANE Select | ENSP00000271628.8:n.34+158T= | |
ENST00000271628.8:c.34+158T= | ENSP00000271628.8:n.34+158T= | |
ENST00000457312.1:c.-232T= | ENSP00000391114.1:n.-232T= | |
NM_005850.4:c.34+158T= | NP_005841.1:n.34+158T= | |
NM_005850.5:c.34+158T= MANE Select | NP_005841.1:n.34+158T= |