HGVS | Genome Assembly |
---|---|
NC_000017.11:g.16948784C= , CM000679.2:g.16948784C= | GRCh38 |
NC_000017.10:g.16852098C= , CM000679.1:g.16852098C= | GRCh37 |
NC_000017.9:g.16792823C= | NCBI36 |
NG_007281.1:g.28305G= , LRG_120:g.28305G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000261652.7:c.399G= MANE Select | ENSP00000261652.2:p.Ser133= | |
ENST00000261652.6:c.399G= | ENSP00000261652.2:p.Ser133= | |
ENST00000579315.5:c.399G= | ENSP00000464069.1:p.Ser133= | |
ENST00000581616.2:n.402G= | ||
ENST00000582931.5:n.303G= | ||
ENST00000583789.1:c.261G= | ENSP00000462952.1:p.Ser87= | |
ENST00000584950.5:c.261G= | ENSP00000463582.1:p.Ser87= | |
NM_012452.2:c.399G= , LRG_120t1:c.399G= | NP_036584.1:p.Ser133= | |
NM_012452.3:c.399G= MANE Select | NP_036584.1:p.Ser133= |