HGVS | Genome Assembly |
---|---|
NC_000012.12:g.57764527A>C , CM000674.2:g.57764527A>C | GRCh38 |
NC_000012.11:g.58158310A>C , CM000674.1:g.58158310A>C | GRCh37 |
NC_000012.10:g.56444577A>C | NCBI36 |
NG_007076.1:g.7667T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000713544.1:c.1068T>G | ENSP00000518840.1:p.Ala356= | |
ENST00000713545.1:c.1045T>G | ENSP00000518841.1:p.Ser349Ala | |
ENST00000228606.9:c.987T>G MANE Select | ENSP00000228606.4:p.Ala329= | |
ENST00000228606.8:c.987T>G | ENSP00000228606.4:p.Ala329= | |
ENST00000546567.5:c.282T>G | ENSP00000449472.1:p.Ala94= | |
ENST00000547344.5:n.1126T>G | ||
NM_000785.3:c.987T>G | NP_000776.1:p.Ala329= | |
NM_000785.4:c.987T>G MANE Select | NP_000776.1:p.Ala329= |