HGVS | Genome Assembly |
---|---|
NC_000006.12:g.108561597A= , CM000668.2:g.108561597A= | GRCh38 |
NC_000006.11:g.108882800A= , CM000668.1:g.108882800A= | GRCh37 |
NC_000006.10:g.108989493A= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000406360.2:c.389A= MANE Select | ENSP00000385824.1:p.Gln130= | |
ENST00000343882.10:c.389A= | ENSP00000339527.6:p.Gln130= | |
ENST00000406360.1:c.389A= | ENSP00000385824.1:p.Gln130= | |
NM_001455.3:c.389A= | NP_001446.1:p.Gln130= | |
NM_201559.2:c.389A= | NP_963853.1:p.Gln130= | |
NM_001455.4:c.389A= MANE Select | NP_001446.1:p.Gln130= | |
NM_201559.3:c.389A= | NP_963853.1:p.Gln130= |