HGVS | Genome Assembly |
---|---|
NC_000017.11:g.74919890C>A , CM000679.2:g.74919890C>A | GRCh38 |
NC_000017.10:g.72915985C>A , CM000679.1:g.72915985C>A | GRCh37 |
NC_000017.9:g.70427580C>A | NCBI36 |
NG_007882.1:g.8367G>T | |
NG_033062.1:g.616C>A | |
NG_007882.2:g.8374G>T | |
NG_033062.2:g.616C>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000614341.5:c.946G>T MANE Select | ENSP00000480279.1:p.Val316Leu | |
ENST00000579243.1:c.*545G>T | ENSP00000462568.1:n.*545G>T | |
ENST00000614341.4:c.946G>T | ENSP00000480279.1:p.Val316Leu | |
NM_001282489.2:c.637G>T | NP_001269418.1:p.Val213Leu | |
NM_173477.4:c.946G>T | NP_775748.2:p.Val316Leu | |
XM_011524296.1:c.637G>T | XP_011522598.1:p.Val213Leu | |
XM_011524296.2:c.637G>T | XP_011522598.1:p.Val213Leu | |
NM_173477.5:c.946G>T MANE Select | NP_775748.2:p.Val316Leu | |
NM_001282489.3:c.637G>T | NP_001269418.1:p.Val213Leu |