HGVS | Genome Assembly |
---|---|
NC_000012.12:g.57766076T>G , CM000674.2:g.57766076T>G | GRCh38 |
NC_000012.11:g.58159859T>G , CM000674.1:g.58159859T>G | GRCh37 |
NC_000012.10:g.56446126T>G | NCBI36 |
NG_007076.1:g.6118A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000546609.2:n.229A>C | ||
ENST00000713544.1:c.317A>C | ENSP00000518840.1:p.Glu106Ala | |
ENST00000713545.1:c.317A>C | ENSP00000518841.1:p.Glu106Ala | |
ENST00000228606.9:c.317A>C MANE Select | ENSP00000228606.4:p.Glu106Ala | |
ENST00000228606.8:c.317A>C | ENSP00000228606.4:p.Glu106Ala | |
ENST00000546496.1:n.145A>C | ||
ENST00000546609.1:c.229A>C | ||
ENST00000547344.5:n.371A>C | ||
ENST00000552186.1:n.436A>C | ||
NM_000785.3:c.317A>C | NP_000776.1:p.Glu106Ala | |
NM_000785.4:c.317A>C MANE Select | NP_000776.1:p.Glu106Ala |