HGVS | Genome Assembly |
---|---|
NC_000012.12:g.69350132G= , CM000674.2:g.69350132G= | GRCh38 |
NC_000012.11:g.69743912G= , CM000674.1:g.69743912G= | GRCh37 |
NC_000012.10:g.68030179G= | NCBI36 |
NG_008195.1:g.6779G= , LRG_768:g.6779G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000261267.7:c.161G= MANE Select | ENSP00000261267.2:p.Ser54= | |
ENST00000261267.6:c.161G= | ENSP00000261267.2:p.Ser54= | |
ENST00000548839.1:c.161G= | ENSP00000449969.1:p.Ser54= | |
ENST00000549690.1:c.161G= | ENSP00000449898.1:p.Ser54= | |
NM_000239.2:c.161G= , LRG_768t1:c.161G= | NP_000230.1:p.Ser54= | |
NM_000239.3:c.161G= MANE Select | NP_000230.1:p.Ser54= |