HGVS | Genome Assembly |
---|---|
NC_000019.10:g.13135703G= , CM000681.2:g.13135703G= | GRCh38 |
NC_000019.9:g.13246517G= , CM000681.1:g.13246517G= | GRCh37 |
NC_000019.8:g.13107517G= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000586171.3:c.496G= | ENSP00000467120.2:p.Val166= | |
ENST00000700232.1:c.496G= | ENSP00000514870.1:p.Val166= | |
ENST00000292431.5:c.496G= MANE Select | ENSP00000292431.3:p.Val166= | |
ENST00000586171.2:c.496G= | ||
ENST00000292431.4:c.496G= | ENSP00000292431.3:p.Val166= | |
ENST00000586171.1:c.496G= | ||
NM_052876.3:c.496G= | NP_443108.1:p.Val166= | |
XM_005259721.2:c.496G= | XP_005259778.1:p.Val166= | |
XM_005259721.3:c.496G= | XP_005259778.1:p.Val166= | |
NM_052876.4:c.496G= MANE Select | NP_443108.1:p.Val166= |