HGVS | Genome Assembly |
---|---|
NC_000008.11:g.118110135C= , CM000670.2:g.118110135C= | GRCh38 |
NC_000008.10:g.119122374C= , CM000670.1:g.119122374C= | GRCh37 |
NC_000008.9:g.119191555C= | NCBI36 |
NG_007455.2:g.6685G= , LRG_493:g.6685G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000378204.7:c.912G= MANE Select | ENSP00000367446.3:p.Trp304= | |
ENST00000436216.2:c.280G= | ||
ENST00000378204.6:c.912G= | ENSP00000367446.2:p.Trp304= | |
ENST00000436216.1:c.280G= | ||
ENST00000437196.1:c.73+839G= | ENSP00000407299.1:n.73+839G= | |
NM_000127.2:c.912G= , LRG_493t1:c.912G= | NP_000118.2:p.Trp304= | |
NM_000127.3:c.912G= MANE Select | NP_000118.2:p.Trp304= |