HGVS | Genome Assembly |
---|---|
NC_000009.12:g.124503331C= , CM000671.2:g.124503331C= | GRCh38 |
NC_000009.11:g.127265610C= , CM000671.1:g.127265610C= | GRCh37 |
NC_000009.10:g.126305431C= | NCBI36 |
NG_008176.1:g.9090G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373588.9:c.65G= MANE Select | ENSP00000362690.4:p.Gly22= | |
ENST00000373588.8:c.65G= | ENSP00000362690.4:p.Gly22= | |
ENST00000455734.1:c.65G= | ENSP00000393245.1:p.Gly22= | |
ENST00000620110.4:c.65G= | ENSP00000483309.1:p.Gly22= | |
NM_004959.4:c.65G= | NP_004950.2:p.Gly22= | |
XM_005251871.2:c.65G= | XP_005251928.1:p.Gly22= | |
XM_005251872.3:c.-55G= | XP_005251929.1:n.-55G= | |
XM_011518455.1:c.65G= | XP_011516757.1:p.Gly22= | |
XM_011518456.1:c.65G= | XP_011516758.1:p.Gly22= | |
NM_004959.5:c.65G= MANE Select | NP_004950.2:p.Gly22= |