HGVS | Genome Assembly |
---|---|
NC_000004.12:g.24800166C= , CM000666.2:g.24800166C= | GRCh38 |
NC_000004.11:g.24801788C= , CM000666.1:g.24801788C= | GRCh37 |
NC_000004.10:g.24410886C= | NCBI36 |
NG_012213.1:g.9704C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382120.4:c.645C= MANE Select | ENSP00000371554.3:p.Pro215= | |
ENST00000382120.3:c.645C= | ENSP00000371554.3:p.Pro215= | |
NM_003102.2:c.645C= | NP_003093.2:p.Pro215= | |
XR_427488.1:n.835C= | ||
NM_003102.3:c.645C= | NP_003093.2:p.Pro215= | |
NM_003102.4:c.645C= MANE Select | NP_003093.2:p.Pro215= |