HGVS | Genome Assembly |
---|---|
NC_000016.10:g.88719735G= , CM000678.2:g.88719735G= | GRCh38 |
NC_000016.9:g.88786143G= , CM000678.1:g.88786143G= | GRCh37 |
NC_000016.8:g.87313644G= | NCBI36 |
NG_042229.1:g.70486C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000301015.14:c.6324-14C= MANE Select | ENSP00000301015.9:n.6324-14C= | |
ENST00000466823.3:c.350-14C= | ||
ENST00000301015.13:c.6324-14C= | ENSP00000301015.9:n.6324-14C= | |
ENST00000419505.5:c.90-14C= | ENSP00000406358.1:n.90-14C= | |
ENST00000466823.2:c.350-14C= | ||
ENST00000495568.7:n.565-14C= | ||
ENST00000497793.2:n.479-14C= | ||
NM_001142864.2:c.6324-14C= | NP_001136336.2:n.6324-14C= | |
NM_001142864.3:c.6324-14C= | NP_001136336.2:n.6324-14C= | |
NM_001142864.4:c.6324-14C= MANE Select | NP_001136336.2:n.6324-14C= |