HGVS | Genome Assembly |
---|---|
NC_000017.11:g.14069514C= , CM000679.2:g.14069514C= | GRCh38 |
NC_000017.10:g.13972831C= , CM000679.1:g.13972831C= | GRCh37 |
NC_000017.9:g.13913556C= | NCBI36 |
NG_008034.1:g.5113C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000261643.8:c.-92C= MANE Select | ENSP00000261643.3:n.-92C= | |
ENST00000664217.1:c.-92C= | ENSP00000499396.1:n.-92C= | |
ENST00000670279.1:c.-92C= | ENSP00000499450.1:n.-92C= | |
ENST00000429152.6:c.-92C= | ENSP00000397750.2:n.-92C= | |
NM_001303.3:c.-92C= | NP_001294.2:n.-92C= | |
XM_005256458.1:c.-92C= | XP_005256515.1:n.-92C= | |
XM_011523657.1:c.-92C= | XP_011521959.1:n.-92C= | |
XM_011523658.1:c.-543C= | XP_011521960.1:n.-543C= | |
XR_933974.1:n.12C= | ||
XR_933975.1:n.12C= | ||
NM_001303.4:c.-92C= MANE Select | NP_001294.2:n.-92C= |