HGVS | Genome Assembly |
---|---|
NC_000008.11:g.117837158C= , CM000670.2:g.117837158C= | GRCh38 |
NC_000008.10:g.118849397C= , CM000670.1:g.118849397C= | GRCh37 |
NC_000008.9:g.118918578C= | NCBI36 |
NG_007455.2:g.279662G= , LRG_493:g.279662G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000684189.1:n.473G= | ||
ENST00000378204.7:c.1006G= MANE Select | ENSP00000367446.3:p.Val336= | |
ENST00000436216.2:c.374G= | ||
ENST00000378204.6:c.1006G= | ENSP00000367446.2:p.Val336= | |
ENST00000436216.1:c.374G= | ||
ENST00000437196.1:c.74-1607G= | ENSP00000407299.1:n.74-1607G= | |
NM_000127.2:c.1006G= , LRG_493t1:c.1006G= | NP_000118.2:p.Val336= | |
NM_000127.3:c.1006G= MANE Select | NP_000118.2:p.Val336= |