HGVS | Genome Assembly |
---|---|
NC_000009.12:g.124503387A>G , CM000671.2:g.124503387A>G | GRCh38 |
NC_000009.11:g.127265666A>G , CM000671.1:g.127265666A>G | GRCh37 |
NC_000009.10:g.126305487A>G | NCBI36 |
NG_008176.1:g.9034T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373588.9:c.9T>C MANE Select | ENSP00000362690.4:p.Tyr3= | |
ENST00000373588.8:c.9T>C | ENSP00000362690.4:p.Tyr3= | |
ENST00000455734.1:c.9T>C | ENSP00000393245.1:p.Tyr3= | |
ENST00000620110.4:c.9T>C | ENSP00000483309.1:p.Tyr3= | |
NM_004959.4:c.9T>C | NP_004950.2:p.Tyr3= | |
XM_005251871.2:c.9T>C | XP_005251928.1:p.Tyr3= | |
XM_005251872.3:c.-111T>C | XP_005251929.1:n.-111T>C | |
XM_011518455.1:c.9T>C | XP_011516757.1:p.Tyr3= | |
XM_011518456.1:c.9T>C | XP_011516758.1:p.Tyr3= | |
NM_004959.5:c.9T>C MANE Select | NP_004950.2:p.Tyr3= |