HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17022677G= , CM000663.2:g.17022677G= | GRCh38 |
NC_000001.10:g.17349172G= , CM000663.1:g.17349172G= | GRCh37 |
NC_000001.9:g.17221759G= | NCBI36 |
NG_012340.1:g.36494C= , LRG_316:g.36494C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000463045.3:c.525C= | ENSP00000481376.2:p.Ala175= | |
ENST00000491274.6:c.654C= | ENSP00000480482.2:p.Ala218= | |
ENST00000375499.8:c.696C= MANE Select | ENSP00000364649.3:p.Ala232= | |
ENST00000375499.7:c.696C= | ENSP00000364649.3:p.Ala232= | |
ENST00000475049.5:n.121C= | ||
ENST00000485092.5:n.360C= | ||
ENST00000485515.5:n.630C= | ||
NM_003000.2:c.696C= , LRG_316t1:c.696C= | NP_002991.2:p.Ala232= | |
NM_003000.3:c.696C= MANE Select | NP_002991.2:p.Ala232= |