HGVS | Genome Assembly |
---|---|
NC_000004.12:g.52038034G= , CM000666.2:g.52038034G= | GRCh38 |
NC_000004.11:g.52904200G= , CM000666.1:g.52904200G= | GRCh37 |
NC_000004.10:g.52598957G= | NCBI36 |
NG_008891.1:g.5286C= , LRG_204:g.5286C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000381431.10:c.33+193C= MANE Select | ENSP00000370839.6:n.33+193C= | |
ENST00000381431.9:c.33+193C= | ENSP00000370839.5:n.33+193C= | |
ENST00000506357.5:c.19+193C= | ||
NM_000232.4:c.33+193C= , LRG_204t1:c.33+193C= | NP_000223.1:n.33+193C= | |
XM_011534403.1:c.33+193C= | XP_011532705.1:n.33+193C= | |
NM_000232.5:c.33+193C= MANE Select | NP_000223.1:n.33+193C= |