HGVS | Genome Assembly |
---|---|
NC_000009.12:g.38396550C>G , CM000671.2:g.38396550C>G | GRCh38 |
NC_000009.11:g.38396547C>G , CM000671.1:g.38396547C>G | GRCh37 |
NC_000009.10:g.38386547C>G | NCBI36 |
NG_012253.1:g.8846C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000377698.4:c.802C>G MANE Select | ENSP00000366927.3:p.His268Asp | |
ENST00000377698.3:c.802C>G | ENSP00000366927.3:p.His268Asp | |
NM_000692.4:c.802C>G | NP_000683.3:p.His268Asp | |
XM_011517802.1:c.802C>G | XP_011516104.1:p.His268Asp | |
XM_011517802.2:c.802C>G | XP_011516104.1:p.His268Asp | |
NM_000692.5:c.802C>G MANE Select | NP_000683.3:p.His268Asp |