HGVS | Genome Assembly |
---|---|
NC_000010.11:g.87727487A>G , CM000672.2:g.87727487A>G | GRCh38 |
NC_000010.10:g.89487244A>G , CM000672.1:g.89487244A>G | GRCh37 |
NC_000010.9:g.89477224A>G | NCBI36 |
NG_012150.1:g.72769A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000456849.2:c.1084A>G MANE Select | ENSP00000406157.1:p.Lys362Glu | |
ENST00000361175.8:c.1069A>G | ENSP00000354436.4:p.Lys357Glu | |
ENST00000456849.1:c.1084A>G | ENSP00000406157.1:p.Lys362Glu | |
NM_001015880.1:c.1084A>G | NP_001015880.1:p.Lys362Glu | |
NM_004670.3:c.1069A>G | NP_004661.2:p.Lys357Glu | |
NM_001015880.2:c.1084A>G MANE Select | NP_001015880.1:p.Lys362Glu | |
NM_004670.4:c.1069A>G | NP_004661.2:p.Lys357Glu |