HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17022684C= , CM000663.2:g.17022684C= | GRCh38 |
NC_000001.10:g.17349179C= , CM000663.1:g.17349179C= | GRCh37 |
NC_000001.9:g.17221766C= | NCBI36 |
NG_012340.1:g.36487G= , LRG_316:g.36487G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000463045.3:c.518G= | ENSP00000481376.2:p.Arg173= | |
ENST00000491274.6:c.647G= | ENSP00000480482.2:p.Arg216= | |
ENST00000375499.8:c.689G= MANE Select | ENSP00000364649.3:p.Arg230= | |
ENST00000375499.7:c.689G= | ENSP00000364649.3:p.Arg230= | |
ENST00000475049.5:n.114G= | ||
ENST00000485092.5:n.353G= | ||
ENST00000485515.5:n.623G= | ||
NM_003000.2:c.689G= , LRG_316t1:c.689G= | NP_002991.2:p.Arg230= | |
NM_003000.3:c.689G= MANE Select | NP_002991.2:p.Arg230= |