HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31860482C= , CM000668.2:g.31860482C= | GRCh38 |
NC_000006.11:g.31828259C= , CM000668.1:g.31828259C= | GRCh37 |
NC_000006.10:g.31936238C= | NCBI36 |
NG_008201.1:g.7451G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375631.5:c.755G= MANE Select | ENSP00000364782.4:p.Gly252= | |
ENST00000677054.1:n.1998G= | ||
ENST00000677512.1:n.863G= | ||
ENST00000678869.1:n.1429G= | ||
ENST00000375631.4:c.755G= | ENSP00000364782.4:p.Gly252= | |
ENST00000480384.1:n.784G= | ||
ENST00000491768.5:c.755G= | ENSP00000433127.1:p.Gly252= | |
ENST00000495807.1:n.1889G= | ||
NM_000434.3:c.755G= | NP_000425.1:p.Gly252= | |
NM_000434.4:c.755G= MANE Select | NP_000425.1:p.Gly252= |