HGVS | Genome Assembly |
---|---|
NC_000008.11:g.23212117T>A , CM000670.2:g.23212117T>A | GRCh38 |
NC_000008.10:g.23069630T>A , CM000670.1:g.23069630T>A | GRCh37 |
NC_000008.9:g.23125575T>A | NCBI36 |
NG_032107.1:g.18051A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000221132.8:c.402A>T MANE Select | ENSP00000221132.3:p.Pro134= | |
ENST00000221132.7:c.402A>T | ENSP00000221132.3:p.Pro134= | |
ENST00000524158.5:c.-205A>T | ENSP00000428884.1:n.-205A>T | |
ENST00000613472.1:c.32-9458A>T | ENSP00000480778.1:n.32-9458A>T | |
NM_003844.3:c.402A>T | NP_003835.3:p.Pro134= | |
NM_003844.4:c.402A>T MANE Select | NP_003835.3:p.Pro134= |