HGVS | Genome Assembly |
---|---|
NC_000011.10:g.92972061G= , CM000673.2:g.92972061G= | GRCh38 |
NC_000011.9:g.92705227G= , CM000673.1:g.92705227G= | GRCh37 |
NC_000011.8:g.92344875G= | NCBI36 |
NG_028160.1:g.7439G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000257068.3:c.223+2113G= MANE Select | ENSP00000257068.2:n.223+2113G= | |
ENST00000257068.2:c.223+2113G= | ENSP00000257068.2:n.223+2113G= | |
ENST00000528076.1:c.165+2113G= | ||
ENST00000532482.1:c.224-400G= | ENSP00000436101.1:n.224-400G= | |
NM_005959.3:c.223+2113G= | NP_005950.1:n.223+2113G= | |
XM_011542839.1:c.223+2113G= | XP_011541141.1:n.223+2113G= | |
XM_011542839.2:c.223+2113G= | XP_011541141.1:n.223+2113G= | |
NM_005959.5:c.223+2113G= MANE Select | NP_005950.1:n.223+2113G= |