HGVS | Genome Assembly |
---|---|
NC_000014.9:g.36663057G>A , CM000676.2:g.36663057G>A | GRCh38 |
NC_000014.8:g.37132262G>A , CM000676.1:g.37132262G>A | GRCh37 |
NC_000014.7:g.36202013G>A | NCBI36 |
NG_013357.1:g.10490G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361487.7:c.165G>A MANE Select | ENSP00000355245.6:p.Lys55= | |
ENST00000555639.2:c.165G>A | ENSP00000501203.1:p.Lys55= | |
ENST00000361487.6:c.165G>A | ENSP00000355245.6:p.Lys55= | |
ENST00000402703.6:c.165G>A | ENSP00000384817.2:p.Lys55= | |
ENST00000554201.1:c.-397G>A | ENSP00000450434.1:n.-397G>A | |
ENST00000555639.1:n.467G>A | ||
NM_006194.3:c.165G>A | NP_006185.1:p.Lys55= | |
NM_001372076.1:c.165G>A MANE Select | NP_001359005.1:p.Lys55= | |
NM_006194.4:c.165G>A | NP_006185.1:p.Lys55= |