HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17028711G= , CM000663.2:g.17028711G= | GRCh38 |
NC_000001.10:g.17355206G= , CM000663.1:g.17355206G= | GRCh37 |
NC_000001.9:g.17227793G= | NCBI36 |
NG_012340.1:g.30460C= , LRG_316:g.30460C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000463045.3:c.141C= | ENSP00000481376.2:p.Asn47= | |
ENST00000491274.6:c.270C= | ENSP00000480482.2:p.Asn90= | |
ENST00000375499.8:c.312C= MANE Select | ENSP00000364649.3:p.Asn104= | |
ENST00000375499.7:c.312C= | ENSP00000364649.3:p.Asn104= | |
ENST00000463045.2:c.141C= | ENSP00000481376.1:p.Asn47= | |
ENST00000475506.1:n.229C= | ||
ENST00000485515.5:n.300C= | ||
ENST00000491274.5:c.270C= | ENSP00000480482.1:p.Asn90= | |
NM_003000.2:c.312C= , LRG_316t1:c.312C= | NP_002991.2:p.Asn104= | |
NM_003000.3:c.312C= MANE Select | NP_002991.2:p.Asn104= |