HGVS | Genome Assembly |
---|---|
NC_000017.11:g.39666051C= , CM000679.2:g.39666051C= | GRCh38 |
NC_000017.10:g.37822304C= , CM000679.1:g.37822304C= | GRCh37 |
NC_000017.9:g.35075830C= | NCBI36 |
NG_008892.1:g.5706C= , LRG_210:g.5706C= | |
NG_042278.1:g.3071C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000309889.3:c.446C= MANE Select | ENSP00000312624.2:p.Pro149= | |
ENST00000309889.2:c.446C= | ENSP00000312624.2:p.Pro149= | |
ENST00000578283.1:c.374C= | ENSP00000462787.1:p.Pro125= | |
NM_003673.3:c.446C= , LRG_210t1:c.446C= | NP_003664.1:p.Pro149= | |
NM_003673.4:c.446C= MANE Select | NP_003664.1:p.Pro149= |