HGVS | Genome Assembly |
---|---|
NC_000007.14:g.30968888G= , CM000669.2:g.30968888G= | GRCh38 |
NC_000007.13:g.31008503G= , CM000669.1:g.31008503G= | GRCh37 |
NC_000007.12:g.30975028G= | NCBI36 |
NG_021416.1:g.9868G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000326139.7:c.112G= MANE Select | ENSP00000320180.2:p.Glu38= | |
ENST00000326139.6:c.112G= | ENSP00000320180.2:p.Glu38= | |
NM_000823.3:c.112G= | NP_000814.2:p.Glu38= | |
NM_000823.4:c.112G= MANE Select | NP_000814.2:p.Glu38= |