HGVS | Genome Assembly |
---|---|
NC_000002.12:g.202556139A= , CM000664.2:g.202556139A= | GRCh38 |
NC_000002.11:g.203420862A= , CM000664.1:g.203420862A= | GRCh37 |
NC_000002.10:g.203129107A= | NCBI36 |
NG_009363.1:g.184813A= , LRG_712:g.184813A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000374580.10:c.2474A= MANE Select | ENSP00000363708.4:p.Tyr825= | |
ENST00000638587.1:c.2405A= | ENSP00000491062.1:n.2405A= | |
ENST00000374574.2:c.1586+3251A= | ENSP00000363702.2:n.1586+3251A= | |
ENST00000374580.8:c.2474A= | ENSP00000363708.4:p.Tyr825= | |
NM_001204.6:c.2474A= , LRG_712t1:c.2474A= | NP_001195.2:p.Tyr825= | |
XM_011511687.1:c.2474A= | XP_011509989.1:p.Tyr825= | |
XM_011511688.1:c.1586+3251A= | XP_011509990.1:n.1586+3251A= | |
NM_001204.7:c.2474A= MANE Select | NP_001195.2:p.Tyr825= |