HGVS | Genome Assembly |
---|---|
NC_000001.11:g.196996129G>C , CM000663.2:g.196996129G>C | GRCh38 |
NC_000001.10:g.196965259G>C , CM000663.1:g.196965259G>C | GRCh37 |
NC_000001.9:g.195231882G>C | NCBI36 |
NG_016365.1:g.23593G>C , LRG_227:g.23593G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000699466.1:c.643G>C | ENSP00000514393.1:p.Glu215Gln | |
ENST00000699467.1:n.967G>C | ||
ENST00000699468.1:c.-9G>C | ENSP00000514394.1:n.-9G>C | |
ENST00000256785.5:c.898G>C MANE Select | ENSP00000256785.4:p.Glu300Gln | |
ENST00000256785.4:c.898G>C | ENSP00000256785.4:p.Glu300Gln | |
NM_030787.3:c.898G>C , LRG_227t1:c.898G>C | NP_110414.1:p.Glu300Gln | |
XM_011510020.1:c.907G>C | XP_011508322.1:p.Glu303Gln | |
XM_011510020.2:c.907G>C | XP_011508322.1:p.Glu303Gln | |
NM_030787.4:c.898G>C MANE Select | NP_110414.1:p.Glu300Gln |