HGVS | Genome Assembly |
---|---|
NC_000014.9:g.36663066G= , CM000676.2:g.36663066G= | GRCh38 |
NC_000014.8:g.37132271G= , CM000676.1:g.37132271G= | GRCh37 |
NC_000014.7:g.36202022G= | NCBI36 |
NG_013357.1:g.10499G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361487.7:c.174G= MANE Select | ENSP00000355245.6:p.Ala58= | |
ENST00000555639.2:c.174G= | ENSP00000501203.1:p.Ala58= | |
ENST00000361487.6:c.174G= | ENSP00000355245.6:p.Ala58= | |
ENST00000402703.6:c.174G= | ENSP00000384817.2:p.Ala58= | |
ENST00000554201.1:c.-388G= | ENSP00000450434.1:n.-388G= | |
ENST00000555639.1:n.476G= | ||
NM_006194.3:c.174G= | NP_006185.1:p.Ala58= | |
NM_001372076.1:c.174G= MANE Select | NP_001359005.1:p.Ala58= | |
NM_006194.4:c.174G= | NP_006185.1:p.Ala58= |