HGVS | Genome Assembly |
---|---|
NC_000016.10:g.88719668C>A , CM000678.2:g.88719668C>A | GRCh38 |
NC_000016.9:g.88786076C>A , CM000678.1:g.88786076C>A | GRCh37 |
NC_000016.8:g.87313577C>A | NCBI36 |
NG_042229.1:g.70553G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000301015.14:c.6377G>T MANE Select | ENSP00000301015.9:p.Trp2126Leu | |
ENST00000466823.3:c.403G>T | ||
ENST00000301015.13:c.6377G>T | ENSP00000301015.9:p.Trp2126Leu | |
ENST00000419505.5:c.143G>T | ENSP00000406358.1:p.Trp48Leu | |
ENST00000466823.2:c.403G>T | ||
ENST00000495568.7:n.618G>T | ||
ENST00000497793.2:n.532G>T | ||
NM_001142864.2:c.6377G>T | NP_001136336.2:p.Trp2126Leu | |
NM_001142864.3:c.6377G>T | NP_001136336.2:p.Trp2126Leu | |
NM_001142864.4:c.6377G>T MANE Select | NP_001136336.2:p.Trp2126Leu |