HGVS | Genome Assembly |
---|---|
NC_000005.10:g.96984663T= , CM000667.2:g.96984663T= | GRCh38 |
NC_000005.9:g.96320367T= , CM000667.1:g.96320367T= | GRCh37 |
NC_000005.8:g.96346123T= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000231368.10:c.861-417T= MANE Select | ENSP00000231368.5:n.861-417T= | |
ENST00000231368.9:c.861-417T= | ENSP00000231368.5:n.861-417T= | |
ENST00000395770.3:c.819-417T= | ENSP00000379117.3:n.819-417T= | |
NM_005575.2:c.861-417T= | NP_005566.2:n.861-417T= | |
NM_175920.3:c.819-417T= | NP_787116.2:n.819-417T= | |
XM_024446045.1:c.861-417T= | XP_024301813.1:n.861-417T= | |
NM_005575.3:c.861-417T= MANE Select | NP_005566.2:n.861-417T= | |
NM_175920.4:c.819-417T= | NP_787116.2:n.819-417T= |