HGVS | Genome Assembly |
---|---|
NC_000008.11:g.117837198A= , CM000670.2:g.117837198A= | GRCh38 |
NC_000008.10:g.118849437A= , CM000670.1:g.118849437A= | GRCh37 |
NC_000008.9:g.118918618A= | NCBI36 |
NG_007455.2:g.279622T= , LRG_493:g.279622T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000684189.1:n.433T= | ||
ENST00000378204.7:c.966T= MANE Select | ENSP00000367446.3:p.Tyr322= | |
ENST00000436216.2:c.334T= | ||
ENST00000378204.6:c.966T= | ENSP00000367446.2:p.Tyr322= | |
ENST00000436216.1:c.334T= | ||
ENST00000437196.1:c.74-1647T= | ENSP00000407299.1:n.74-1647T= | |
NM_000127.2:c.966T= , LRG_493t1:c.966T= | NP_000118.2:p.Tyr322= | |
NM_000127.3:c.966T= MANE Select | NP_000118.2:p.Tyr322= |