HGVS | Genome Assembly |
---|---|
NC_000017.11:g.16972039T= , CM000679.2:g.16972039T= | GRCh38 |
NC_000017.10:g.16875353T= , CM000679.1:g.16875353T= | GRCh37 |
NC_000017.9:g.16816078T= | NCBI36 |
NG_007281.1:g.5050A= , LRG_120:g.5050A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261652.7:c.37A= MANE Select | ENSP00000261652.2:p.Ser13= | |
ENST00000261652.6:c.37A= | ENSP00000261652.2:p.Ser13= | |
ENST00000579315.5:c.37A= | ENSP00000464069.1:p.Ser13= | |
ENST00000581616.2:n.40A= | ||
ENST00000582931.5:n.79A= | ||
ENST00000583789.1:c.37A= | ENSP00000462952.1:p.Ser13= | |
ENST00000584950.5:c.37A= | ENSP00000463582.1:p.Ser13= | |
NM_012452.2:c.37A= , LRG_120t1:c.37A= | NP_036584.1:p.Ser13= | |
NM_012452.3:c.37A= MANE Select | NP_036584.1:p.Ser13= |