HGVS | Genome Assembly |
---|---|
NC_000019.10:g.35848076C= , CM000681.2:g.35848076C= | GRCh38 |
NC_000019.9:g.36338978C= , CM000681.1:g.36338978C= | GRCh37 |
NC_000019.8:g.41030818C= | NCBI36 |
NG_013356.2:g.26212G= , LRG_693:g.26212G= | |
NG_051206.1:g.1442C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378910.10:c.1405G= MANE Select | ENSP00000368190.4:p.Gly469= | |
ENST00000353632.6:c.1405G= | ENSP00000343634.5:p.Gly469= | |
ENST00000378910.9:c.1405G= | ENSP00000368190.4:p.Gly469= | |
ENST00000592132.1:n.412G= | ||
NM_004646.3:c.1405G= , LRG_693t1:c.1405G= | NP_004637.1:p.Gly469= | |
NM_004646.4:c.1405G= MANE Select | NP_004637.1:p.Gly469= |