HGVS | Genome Assembly |
---|---|
NC_000010.11:g.93588381T>A , CM000672.2:g.93588381T>A | GRCh38 |
NC_000010.10:g.95348138T>A , CM000672.1:g.95348138T>A | GRCh37 |
NC_000010.9:g.95338128T>A | NCBI36 |
NG_032670.1:g.26717T>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000371481.9:c.*772T>A MANE Select | ENSP00000360536.5:n.*772T>A | |
ENST00000371481.8:c.*772T>A | ENSP00000360536.4:n.*772T>A | |
ENST00000371483.8:c.*772T>A | ENSP00000360538.4:n.*772T>A | |
ENST00000604414.1:c.696+12162T>A | ENSP00000474477.1:n.696+12162T>A | |
NM_001195755.1:c.*772T>A | NP_001182684.1:n.*772T>A | |
NM_181745.3:c.*772T>A | NP_859529.2:n.*772T>A | |
NM_001195755.2:c.*772T>A MANE Select | NP_001182684.1:n.*772T>A | |
NM_181745.4:c.*772T>A | NP_859529.2:n.*772T>A |