HGVS | Genome Assembly |
---|---|
NC_000016.10:g.88719675A= , CM000678.2:g.88719675A= | GRCh38 |
NC_000016.9:g.88786083A= , CM000678.1:g.88786083A= | GRCh37 |
NC_000016.8:g.87313584A= | NCBI36 |
NG_042229.1:g.70546T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000301015.14:c.6370T= MANE Select | ENSP00000301015.9:p.Trp2124= | |
ENST00000466823.3:c.396T= | ||
ENST00000301015.13:c.6370T= | ENSP00000301015.9:p.Trp2124= | |
ENST00000419505.5:c.136T= | ENSP00000406358.1:p.Trp46= | |
ENST00000466823.2:c.396T= | ||
ENST00000495568.7:n.611T= | ||
ENST00000497793.2:n.525T= | ||
NM_001142864.2:c.6370T= | NP_001136336.2:p.Trp2124= | |
NM_001142864.3:c.6370T= | NP_001136336.2:p.Trp2124= | |
NM_001142864.4:c.6370T= MANE Select | NP_001136336.2:p.Trp2124= |