HGVS | Genome Assembly |
---|---|
NC_000001.11:g.149927554C= , CM000663.2:g.149927554C= | GRCh38 |
NC_000001.10:g.149899446C= , CM000663.1:g.149899446C= | GRCh37 |
NC_000001.9:g.148166070C= | NCBI36 |
NG_032777.1:g.5699G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000271628.9:c.34+172G= MANE Select | ENSP00000271628.8:n.34+172G= | |
ENST00000271628.8:c.34+172G= | ENSP00000271628.8:n.34+172G= | |
ENST00000457312.1:c.-218G= | ENSP00000391114.1:n.-218G= | |
NM_005850.4:c.34+172G= | NP_005841.1:n.34+172G= | |
NM_005850.5:c.34+172G= MANE Select | NP_005841.1:n.34+172G= |