HGVS | Genome Assembly |
---|---|
NC_000004.12:g.24800031G= , CM000666.2:g.24800031G= | GRCh38 |
NC_000004.11:g.24801653G= , CM000666.1:g.24801653G= | GRCh37 |
NC_000004.10:g.24410751G= | NCBI36 |
NG_012213.1:g.9569G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382120.4:c.510G= MANE Select | ENSP00000371554.3:p.Pro170= | |
ENST00000382120.3:c.510G= | ENSP00000371554.3:p.Pro170= | |
NM_003102.2:c.510G= | NP_003093.2:p.Pro170= | |
XR_427488.1:n.700G= | ||
NM_003102.3:c.510G= | NP_003093.2:p.Pro170= | |
NM_003102.4:c.510G= MANE Select | NP_003093.2:p.Pro170= |