HGVS | Genome Assembly |
---|---|
NC_000012.12:g.8648056C>T , CM000674.2:g.8648056C>T | GRCh38 |
NC_000012.11:g.8800652C>T , CM000674.1:g.8800652C>T | GRCh37 |
NC_000012.10:g.8691919C>T | NCBI36 |
NG_041814.1:g.19833G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000359478.7:c.*35G>A MANE Select | ENSP00000352455.2:n.*35G>A | |
ENST00000359478.6:c.*35G>A | ENSP00000352455.2:n.*35G>A | |
ENST00000396549.6:c.*35G>A | ENSP00000379798.2:n.*35G>A | |
ENST00000433590.6:c.*35G>A | ENSP00000411997.2:n.*35G>A | |
ENST00000535336.5:c.*35G>A | ENSP00000438525.1:n.*35G>A | |
ENST00000535411.5:c.520+6G>A | ||
ENST00000543369.5:c.*35G>A | ENSP00000441492.1:n.*35G>A | |
ENST00000543467.5:c.269+6G>A | ENSP00000444531.1:n.269+6G>A | |
ENST00000544211.5:c.*209G>A | ENSP00000443839.1:n.*209G>A | |
NM_001297709.1:c.*35G>A | NP_001284638.1:n.*35G>A | |
NM_001297710.1:c.*35G>A | NP_001284639.1:n.*35G>A | |
NM_001297711.1:c.*35G>A | NP_001284640.1:n.*35G>A | |
NM_001297712.1:c.*35G>A | NP_001284641.1:n.*35G>A | |
NM_003480.3:c.*35G>A | NP_003471.1:n.*35G>A | |
NR_123733.1:n.890G>A | ||
NR_123734.1:n.860G>A | ||
NM_003480.4:c.*35G>A MANE Select | NP_003471.1:n.*35G>A | |
NM_001297709.2:c.*35G>A | NP_001284638.1:n.*35G>A | |
NM_001297710.2:c.*35G>A | NP_001284639.1:n.*35G>A | |
NM_001297711.2:c.*35G>A | NP_001284640.1:n.*35G>A | |
NM_001297712.2:c.*35G>A | NP_001284641.1:n.*35G>A | |
NR_123733.2:n.828G>A | ||
NR_123734.2:n.798G>A |