HGVS | Genome Assembly |
---|---|
NC_000002.12:g.202467617T= , CM000664.2:g.202467617T= | GRCh38 |
NC_000002.11:g.203332340T= , CM000664.1:g.203332340T= | GRCh37 |
NC_000002.10:g.203040585T= | NCBI36 |
NG_009363.1:g.96291T= , LRG_712:g.96291T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000374580.10:c.346T= MANE Select | ENSP00000363708.4:p.Cys116= | |
ENST00000638587.1:c.277T= | ENSP00000491062.1:p.Cys93= | |
ENST00000374574.2:c.346T= | ENSP00000363702.2:p.Cys116= | |
ENST00000374580.8:c.346T= | ENSP00000363708.4:p.Cys116= | |
ENST00000479069.1:n.253T= | ||
NM_001204.6:c.346T= , LRG_712t1:c.346T= | NP_001195.2:p.Cys116= | |
XM_011511687.1:c.346T= | XP_011509989.1:p.Cys116= | |
XM_011511688.1:c.346T= | XP_011509990.1:p.Cys116= | |
NM_001204.7:c.346T= MANE Select | NP_001195.2:p.Cys116= |