HGVS | Genome Assembly |
---|---|
NC_000001.11:g.1014081A>T , CM000663.2:g.1014081A>T | GRCh38 |
NC_000001.10:g.949461A>T , CM000663.1:g.949461A>T | GRCh37 |
NC_000001.9:g.939324A>T | NCBI36 |
NG_033033.1:g.5615A>T | |
NG_033033.2:g.17944A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000624697.4:c.77A>T | ENSP00000485643.1:p.Gln26Leu | |
ENST00000649529.1:c.101A>T MANE Select | ENSP00000496832.1:p.Gln34Leu | |
ENST00000379389.4:c.101A>T | ENSP00000368699.4:p.Gln34Leu | |
ENST00000624652.1:c.77A>T | ENSP00000485313.1:p.Gln26Leu | |
ENST00000624697.3:c.77A>T | ENSP00000485643.1:p.Gln26Leu | |
NM_005101.3:c.101A>T | NP_005092.1:p.Gln34Leu | |
NM_005101.4:c.101A>T MANE Select | NP_005092.1:p.Gln34Leu |