HGVS | Genome Assembly |
---|---|
NC_000012.12:g.65170137G>A , CM000674.2:g.65170137G>A | GRCh38 |
NC_000012.11:g.65563917G>A , CM000674.1:g.65563917G>A | GRCh37 |
NC_000012.10:g.63850184G>A | NCBI36 |
NG_016210.1:g.5567G>A | |
NG_016210.2:g.5567G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000308330.3:c.541G>A MANE Select | ENSP00000308369.2:p.Glu181Lys | |
ENST00000308330.2:c.541G>A | ENSP00000308369.2:p.Glu181Lys | |
ENST00000541171.1:n.555G>A | ||
NM_001167614.1:c.541G>A | NP_001161086.1:p.Glu181Lys | |
NM_014319.4:c.541G>A | NP_055134.2:p.Glu181Lys | |
NM_014319.5:c.541G>A MANE Select | NP_055134.2:p.Glu181Lys | |
NM_001167614.2:c.541G>A | NP_001161086.1:p.Glu181Lys |