HGVS | Genome Assembly |
---|---|
NC_000008.11:g.118110096G= , CM000670.2:g.118110096G= | GRCh38 |
NC_000008.10:g.119122335G= , CM000670.1:g.119122335G= | GRCh37 |
NC_000008.9:g.119191516G= | NCBI36 |
NG_007455.2:g.6724C= , LRG_493:g.6724C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000378204.7:c.951C= MANE Select | ENSP00000367446.3:p.Thr317= | |
ENST00000436216.2:c.319C= | ||
ENST00000378204.6:c.951C= | ENSP00000367446.2:p.Thr317= | |
ENST00000436216.1:c.319C= | ||
ENST00000437196.1:c.73+878C= | ENSP00000407299.1:n.73+878C= | |
NM_000127.2:c.951C= , LRG_493t1:c.951C= | NP_000118.2:p.Thr317= | |
NM_000127.3:c.951C= MANE Select | NP_000118.2:p.Thr317= |