HGVS | Genome Assembly |
---|---|
NC_000002.12:g.46306267T= , CM000664.2:g.46306267T= | GRCh38 |
NC_000002.11:g.46533406T= , CM000664.1:g.46533406T= | GRCh37 |
NC_000002.10:g.46386910T= | NCBI36 |
NG_016000.1:g.13866T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000263734.5:c.26+8330T= MANE Select | ENSP00000263734.3:n.26+8330T= | |
ENST00000263734.4:c.26+8330T= | ENSP00000263734.3:n.26+8330T= | |
ENST00000449347.5:c.26+8330T= | ENSP00000406137.1:n.26+8330T= | |
ENST00000460015.1:n.432+12169T= | ||
ENST00000467888.5:n.174+8330T= | ||
NM_001430.4:c.26+8330T= | NP_001421.2:n.26+8330T= | |
XR_940055.1:n.2501+7826A= | ||
NM_001430.5:c.26+8330T= MANE Select | NP_001421.2:n.26+8330T= |