HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31860468C= , CM000668.2:g.31860468C= | GRCh38 |
NC_000006.11:g.31828245C= , CM000668.1:g.31828245C= | GRCh37 |
NC_000006.10:g.31936224C= | NCBI36 |
NG_008201.1:g.7465G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000375631.5:c.769G= MANE Select | ENSP00000364782.4:p.Glu257= | |
ENST00000677054.1:n.2012G= | ||
ENST00000677512.1:n.877G= | ||
ENST00000678869.1:n.1443G= | ||
ENST00000375631.4:c.769G= | ENSP00000364782.4:p.Glu257= | |
ENST00000480384.1:n.798G= | ||
ENST00000491768.5:c.769G= | ENSP00000433127.1:p.Glu257= | |
ENST00000495807.1:n.1903G= | ||
NM_000434.3:c.769G= | NP_000425.1:p.Glu257= | |
NM_000434.4:c.769G= MANE Select | NP_000425.1:p.Glu257= |