HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17022637T= , CM000663.2:g.17022637T= | GRCh38 |
NC_000001.10:g.17349132T= , CM000663.1:g.17349132T= | GRCh37 |
NC_000001.9:g.17221719T= | NCBI36 |
NG_012340.1:g.36534A= , LRG_316:g.36534A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000463045.3:c.565A= | ENSP00000481376.2:p.Ile189= | |
ENST00000491274.6:c.694A= | ENSP00000480482.2:p.Ile232= | |
ENST00000375499.8:c.736A= MANE Select | ENSP00000364649.3:p.Ile246= | |
ENST00000375499.7:c.736A= | ENSP00000364649.3:p.Ile246= | |
ENST00000475049.5:n.161A= | ||
ENST00000485092.5:n.400A= | ||
ENST00000485515.5:n.670A= | ||
NM_003000.2:c.736A= , LRG_316t1:c.736A= | NP_002991.2:p.Ile246= | |
NM_003000.3:c.736A= MANE Select | NP_002991.2:p.Ile246= |