HGVS | Genome Assembly |
---|---|
NC_000016.10:g.88719598G>A , CM000678.2:g.88719598G>A | GRCh38 |
NC_000016.9:g.88786006G>A , CM000678.1:g.88786006G>A | GRCh37 |
NC_000016.8:g.87313507G>A | NCBI36 |
NG_042229.1:g.70623C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000301015.14:c.6447C>T MANE Select | ENSP00000301015.9:p.Ile2149= | |
ENST00000466823.3:c.473C>T | ||
ENST00000301015.13:c.6447C>T | ENSP00000301015.9:p.Ile2149= | |
ENST00000419505.5:c.213C>T | ENSP00000406358.1:p.Ile71= | |
ENST00000466823.2:c.473C>T | ||
ENST00000495568.7:n.688C>T | ||
ENST00000497793.2:n.602C>T | ||
NM_001142864.2:c.6447C>T | NP_001136336.2:p.Ile2149= | |
NM_001142864.3:c.6447C>T | NP_001136336.2:p.Ile2149= | |
NM_001142864.4:c.6447C>T MANE Select | NP_001136336.2:p.Ile2149= |