HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17028735G= , CM000663.2:g.17028735G= | GRCh38 |
NC_000001.10:g.17355230G= , CM000663.1:g.17355230G= | GRCh37 |
NC_000001.9:g.17227817G= | NCBI36 |
NG_012340.1:g.30436C= , LRG_316:g.30436C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000463045.3:c.117C= | ENSP00000481376.2:p.Gly39= | |
ENST00000491274.6:c.246C= | ENSP00000480482.2:p.Gly82= | |
ENST00000375499.8:c.288C= MANE Select | ENSP00000364649.3:p.Gly96= | |
ENST00000375499.7:c.288C= | ENSP00000364649.3:p.Gly96= | |
ENST00000463045.2:c.117C= | ENSP00000481376.1:p.Gly39= | |
ENST00000475506.1:n.205C= | ||
ENST00000485515.5:n.276C= | ||
ENST00000491274.5:c.246C= | ENSP00000480482.1:p.Gly82= | |
NM_003000.2:c.288C= , LRG_316t1:c.288C= | NP_002991.2:p.Gly96= | |
NM_003000.3:c.288C= MANE Select | NP_002991.2:p.Gly96= |