HGVS | Genome Assembly |
---|---|
NC_000009.12:g.110668985T>G , CM000671.2:g.110668985T>G | GRCh38 |
NC_000009.11:g.113431265T>G , CM000671.1:g.113431265T>G | GRCh37 |
NC_000009.10:g.112471086T>G | NCBI36 |
NG_016016.1:g.5215T>G | |
NG_016016.2:g.5195T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000374448.9:c.79+2T>G MANE Select | ENSP00000363571.4:n.79+2T>G | |
ENST00000189978.10:c.79+2T>G | ENSP00000189978.6:n.79+2T>G | |
ENST00000374440.7:c.79+2T>G | ENSP00000363563.4:n.79+2T>G | |
ENST00000374448.8:c.79+2T>G | ENSP00000363571.4:n.79+2T>G | |
ENST00000416899.7:c.79+2T>G | ENSP00000393608.3:n.79+2T>G | |
NM_001166280.1:c.79+2T>G | NP_001159752.1:n.79+2T>G | |
NM_001166281.1:c.79+2T>G | NP_001159753.1:n.79+2T>G | |
NM_005592.3:c.79+2T>G | NP_005583.1:n.79+2T>G | |
XM_005251994.2:c.79+2T>G | XP_005252051.1:n.79+2T>G | |
XM_005251995.2:c.79+2T>G | XP_005252052.1:n.79+2T>G | |
XM_005251996.2:c.79+2T>G | XP_005252053.1:n.79+2T>G | |
XM_011518707.1:c.79+2T>G | XP_011517009.1:n.79+2T>G | |
XM_005251994.3:c.79+2T>G | XP_005252051.1:n.79+2T>G | |
XM_005251995.3:c.79+2T>G | XP_005252052.1:n.79+2T>G | |
XM_005251996.3:c.79+2T>G | XP_005252053.1:n.79+2T>G | |
XM_017014734.1:c.79+2T>G | XP_016870223.1:n.79+2T>G | |
NM_001166280.2:c.79+2T>G | NP_001159752.1:n.79+2T>G | |
NM_001166281.2:c.79+2T>G | NP_001159753.1:n.79+2T>G | |
NM_005592.4:c.79+2T>G MANE Select | NP_005583.1:n.79+2T>G |