HGVS | Genome Assembly |
---|---|
NC_000019.10:g.40848233T= , CM000681.2:g.40848233T= | GRCh38 |
NC_000019.9:g.41354138T= , CM000681.1:g.41354138T= | GRCh37 |
NC_000019.8:g.46045978T= | NCBI36 |
NG_008377.1:g.7215A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000301141.10:c.640A= MANE Select | ENSP00000301141.4:p.Thr214= | |
ENST00000301141.9:c.640A= | ENSP00000301141.4:p.Thr214= | |
ENST00000596719.5:n.491A= | ||
ENST00000600495.1:c.*452A= | ENSP00000472905.1:n.*452A= | |
ENST00000601627.1:c.120-43758T= | ||
ENST00000610301.1:c.640A= | ENSP00000477899.1:p.Thr214= | |
NM_000762.5:c.640A= | NP_000753.3:p.Thr214= | |
NM_000762.6:c.640A= MANE Select | NP_000753.3:p.Thr214= |