HGVS | Genome Assembly |
---|---|
NC_000011.10:g.67586527G>A , CM000673.2:g.67586527G>A | GRCh38 |
NC_000011.9:g.67353998G>A , CM000673.1:g.67353998G>A | GRCh37 |
NC_000011.8:g.67110574G>A | NCBI36 |
NG_012075.1:g.7933G>A , LRG_723:g.7933G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000398603.6:c.475G>A | ENSP00000381604.1:p.Ala159Thr | |
ENST00000398606.10:c.583G>A MANE Select | ENSP00000381607.3:p.Ala195Thr | |
ENST00000398603.5:c.475G>A | ENSP00000381604.1:p.Ala159Thr | |
ENST00000398606.7:c.583G>A | ENSP00000381607.3:p.Ala195Thr | |
ENST00000467591.1:n.694G>A | ||
ENST00000494593.1:n.1555G>A | ||
ENST00000498765.5:c.646G>A | ||
NM_000852.3:c.583G>A , LRG_723t1:c.583G>A | NP_000843.1:p.Ala195Thr | |
NM_000852.4:c.583G>A MANE Select | NP_000843.1:p.Ala195Thr |