HGVS | Genome Assembly |
---|---|
NC_000005.10:g.81207121T= , CM000667.2:g.81207121T= | GRCh38 |
NC_000005.9:g.80502940T= , CM000667.1:g.80502940T= | GRCh37 |
NC_000005.8:g.80538696T= | NCBI36 |
NG_030334.1:g.251433T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000265080.9:c.2968-125T= MANE Select | ENSP00000265080.4:n.2968-125T= | |
ENST00000265080.8:c.2968-125T= | ENSP00000265080.4:n.2968-125T= | |
ENST00000503795.1:c.2968-125T= | ENSP00000421771.1:n.2968-125T= | |
NM_006909.2:c.2968-125T= | NP_008840.1:n.2968-125T= | |
XM_017009682.2:c.2683-125T= | XP_016865171.1:n.2683-125T= | |
XR_002956166.1:n.3084-125T= | ||
NM_006909.3:c.2968-125T= MANE Select | NP_008840.1:n.2968-125T= |