HGVS | Genome Assembly |
---|---|
NC_000004.12:g.24799990T= , CM000666.2:g.24799990T= | GRCh38 |
NC_000004.11:g.24801612T= , CM000666.1:g.24801612T= | GRCh37 |
NC_000004.10:g.24410710T= | NCBI36 |
NG_012213.1:g.9528T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382120.4:c.469T= MANE Select | ENSP00000371554.3:p.Trp157= | |
ENST00000382120.3:c.469T= | ENSP00000371554.3:p.Trp157= | |
NM_003102.2:c.469T= | NP_003093.2:p.Trp157= | |
XR_427488.1:n.659T= | ||
NM_003102.3:c.469T= | NP_003093.2:p.Trp157= | |
NM_003102.4:c.469T= MANE Select | NP_003093.2:p.Trp157= |