HGVS | Genome Assembly |
---|---|
NC_000017.11:g.14208508T>C , CM000679.2:g.14208508T>C | GRCh38 |
NC_000017.10:g.14111825T>C , CM000679.1:g.14111825T>C | GRCh37 |
NC_000017.9:g.14052550T>C | NCBI36 |
NG_008034.1:g.144107T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261643.8:c.*1295T>C MANE Select | ENSP00000261643.3:n.*1295T>C | |
ENST00000664217.1:c.*56-46T>C | ENSP00000499396.1:n.*56-46T>C | |
ENST00000670279.1:c.929-1001T>C | ENSP00000499450.1:n.929-1001T>C | |
ENST00000261643.7:c.*1295T>C | ENSP00000261643.3:n.*1295T>C | |
NM_001303.3:c.*1295T>C | NP_001294.2:n.*1295T>C | |
XM_011523658.1:c.*1295T>C | XP_011521960.1:n.*1295T>C | |
XR_933974.1:n.1032-1001T>C | ||
NM_001303.4:c.*1295T>C MANE Select | NP_001294.2:n.*1295T>C |