HGVS | Genome Assembly |
---|---|
NC_000007.14:g.107683292A>G , CM000669.2:g.107683292A>G | GRCh38 |
NC_000007.13:g.107323737A>G , CM000669.1:g.107323737A>G | GRCh37 |
NC_000007.12:g.107110973A>G | NCBI36 |
NG_008489.1:g.27658A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000644269.2:c.856A>G MANE Select | ENSP00000494017.1:p.Lys286Glu | |
ENST00000265715.7:c.856A>G | ENSP00000265715.3:p.Lys286Glu | |
NM_000441.1:c.856A>G | NP_000432.1:p.Lys286Glu | |
XM_005250425.1:c.856A>G | XP_005250482.1:p.Lys286Glu | |
XM_006716025.2:c.856A>G | XP_006716088.1:p.Lys286Glu | |
XM_005250425.2:c.856A>G | XP_005250482.1:p.Lys286Glu | |
XM_006716025.3:c.856A>G | XP_006716088.1:p.Lys286Glu | |
XM_017012318.1:c.856A>G | XP_016867807.1:p.Lys286Glu | |
NM_000441.2:c.856A>G MANE Select | NP_000432.1:p.Lys286Glu |