HGVS | Genome Assembly |
---|---|
NC_000001.11:g.193122122G>A , CM000663.2:g.193122122G>A | GRCh38 |
NC_000001.10:g.193091252G>A , CM000663.1:g.193091252G>A | GRCh37 |
NC_000001.9:g.191357875G>A | NCBI36 |
NG_012691.1:g.5165G>A , LRG_507:g.5165G>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000367435.5:c.-79G>A MANE Select | ENSP00000356405.4:n.-79G>A | |
ENST00000643006.1:c.-79G>A | ENSP00000496633.1:n.-79G>A | |
ENST00000649895.1:n.140G>A | ||
ENST00000650197.1:c.-79G>A | ENSP00000496929.1:n.-79G>A | |
ENST00000367435.3:c.-79G>A | ENSP00000356405.3:n.-79G>A | |
NM_024529.4:c.-79G>A , LRG_507t1:c.-79G>A | NP_078805.3:n.-79G>A | |
XM_006711537.2:c.-79G>A | XP_006711600.1:n.-79G>A | |
XM_006711537.4:c.-79G>A | XP_006711600.1:n.-79G>A | |
XR_001738350.1:n.1535C>T | ||
NM_024529.5:c.-79G>A MANE Select | NP_078805.3:n.-79G>A |