HGVS | Genome Assembly |
---|---|
NC_000012.12:g.65170107A>G , CM000674.2:g.65170107A>G | GRCh38 |
NC_000012.11:g.65563887A>G , CM000674.1:g.65563887A>G | GRCh37 |
NC_000012.10:g.63850154A>G | NCBI36 |
NG_016210.1:g.5537A>G | |
NG_016210.2:g.5537A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000308330.3:c.511A>G MANE Select | ENSP00000308369.2:p.Lys171Glu | |
ENST00000308330.2:c.511A>G | ENSP00000308369.2:p.Lys171Glu | |
ENST00000541171.1:n.525A>G | ||
NM_001167614.1:c.511A>G | NP_001161086.1:p.Lys171Glu | |
NM_014319.4:c.511A>G | NP_055134.2:p.Lys171Glu | |
NM_014319.5:c.511A>G MANE Select | NP_055134.2:p.Lys171Glu | |
NM_001167614.2:c.511A>G | NP_001161086.1:p.Lys171Glu |