HGVS | Genome Assembly |
---|---|
NC_000016.10:g.88719831G>A , CM000678.2:g.88719831G>A | GRCh38 |
NC_000016.9:g.88786239G>A , CM000678.1:g.88786239G>A | GRCh37 |
NC_000016.8:g.87313740G>A | NCBI36 |
NG_042229.1:g.70390C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000301015.14:c.6294C>T MANE Select | ENSP00000301015.9:p.Tyr2098= | |
ENST00000466823.3:c.320C>T | ||
ENST00000301015.13:c.6294C>T | ENSP00000301015.9:p.Tyr2098= | |
ENST00000419505.5:c.60C>T | ENSP00000406358.1:p.Tyr20= | |
ENST00000466823.2:c.320C>T | ||
ENST00000495568.7:n.535C>T | ||
ENST00000497793.2:n.449C>T | ||
NM_001142864.2:c.6294C>T | NP_001136336.2:p.Tyr2098= | |
NM_001142864.3:c.6294C>T | NP_001136336.2:p.Tyr2098= | |
NM_001142864.4:c.6294C>T MANE Select | NP_001136336.2:p.Tyr2098= |