HGVS | Genome Assembly |
---|---|
NC_000012.12:g.57764138T>G , CM000674.2:g.57764138T>G | GRCh38 |
NC_000012.11:g.58157921T>G , CM000674.1:g.58157921T>G | GRCh37 |
NC_000012.10:g.56444188T>G | NCBI36 |
NG_007076.1:g.8056A>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000713544.1:c.1256A>C | ENSP00000518840.1:p.Asp419Ala | |
ENST00000713545.1:c.*180A>C | ENSP00000518841.1:n.*180A>C | |
ENST00000228606.9:c.1175A>C MANE Select | ENSP00000228606.4:p.Asp392Ala | |
ENST00000228606.8:c.1175A>C | ENSP00000228606.4:p.Asp392Ala | |
ENST00000546567.5:c.470A>C | ENSP00000449472.1:p.Asp157Ala | |
ENST00000547344.5:n.1314A>C | ||
NM_000785.3:c.1175A>C | NP_000776.1:p.Asp392Ala | |
NM_000785.4:c.1175A>C MANE Select | NP_000776.1:p.Asp392Ala |