HGVS | Genome Assembly |
---|---|
NC_000001.11:g.23817560T= , CM000663.2:g.23817560T= | GRCh38 |
NC_000001.10:g.24144050T= , CM000663.1:g.24144050T= | GRCh37 |
NC_000001.9:g.24016637T= | NCBI36 |
NG_013061.1:g.12900A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000374490.8:c.168A= MANE Select | ENSP00000363614.3:p.Lys56= | |
ENST00000235958.4:c.131+2950A= | ||
ENST00000374487.6:c.*209A= | ENSP00000363611.2:n.*209A= | |
ENST00000374490.7:c.168A= | ENSP00000363614.3:p.Lys56= | |
ENST00000436439.6:c.168A= | ENSP00000389281.2:p.Lys56= | |
ENST00000509389.5:n.180A= | ||
ENST00000513148.1:n.169A= | ||
NM_000191.2:c.168A= | NP_000182.2:p.Lys56= | |
NM_001166059.1:c.168A= | NP_001159531.1:p.Lys56= | |
NM_000191.3:c.168A= MANE Select | NP_000182.2:p.Lys56= | |
NM_001166059.2:c.168A= | NP_001159531.1:p.Lys56= |