HGVS | Genome Assembly |
---|---|
NC_000012.12:g.57764518C>T , CM000674.2:g.57764518C>T | GRCh38 |
NC_000012.11:g.58158301C>T , CM000674.1:g.58158301C>T | GRCh37 |
NC_000012.10:g.56444568C>T | NCBI36 |
NG_007076.1:g.7676G>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000713544.1:c.1077G>A | ENSP00000518840.1:p.Glu359= | |
ENST00000713545.1:c.*1G>A | ENSP00000518841.1:n.*1G>A | |
ENST00000228606.9:c.996G>A MANE Select | ENSP00000228606.4:p.Glu332= | |
ENST00000228606.8:c.996G>A | ENSP00000228606.4:p.Glu332= | |
ENST00000546567.5:c.291G>A | ENSP00000449472.1:p.Glu97= | |
ENST00000547344.5:n.1135G>A | ||
NM_000785.3:c.996G>A | NP_000776.1:p.Glu332= | |
NM_000785.4:c.996G>A MANE Select | NP_000776.1:p.Glu332= |