HGVS | Genome Assembly |
---|---|
NC_000017.11:g.14208609G= , CM000679.2:g.14208609G= | GRCh38 |
NC_000017.10:g.14111926G= , CM000679.1:g.14111926G= | GRCh37 |
NC_000017.9:g.14052651G= | NCBI36 |
NG_008034.1:g.144208G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261643.8:c.*1396G= MANE Select | ENSP00000261643.3:n.*1396G= | |
ENST00000664217.1:c.*111G= | ENSP00000499396.1:n.*111G= | |
ENST00000670279.1:c.929-900G= | ENSP00000499450.1:n.929-900G= | |
ENST00000261643.7:c.*1396G= | ENSP00000261643.3:n.*1396G= | |
NM_001303.3:c.*1396G= | NP_001294.2:n.*1396G= | |
XM_011523658.1:c.*1396G= | XP_011521960.1:n.*1396G= | |
XR_933974.1:n.1032-900G= | ||
NM_001303.4:c.*1396G= MANE Select | NP_001294.2:n.*1396G= |