HGVS | Genome Assembly |
---|---|
NC_000005.10:g.81206816_81206822del , CM000667.2:g.81206816_81206822del | GRCh38 |
NC_000005.9:g.80502635_80502641del , CM000667.1:g.80502635_80502641del | GRCh37 |
NC_000005.8:g.80538391_80538397del | NCBI36 |
NG_030334.1:g.251128_251134del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000265080.9:c.2907-29_2907-23del MANE Select | ENSP00000265080.4:n.2907-29_2907-23del | |
ENST00000265080.8:c.2907-29_2907-23del | ENSP00000265080.4:n.2907-29_2907-23del | |
ENST00000503795.1:c.2907-29_2907-23del | ENSP00000421771.1:n.2907-29_2907-23del | |
NM_006909.2:c.2907-29_2907-23del | NP_008840.1:n.2907-29_2907-23del | |
XM_017009682.2:c.2622-29_2622-23del | XP_016865171.1:n.2622-29_2622-23del | |
XR_002956166.1:n.3023-29_3023-23del | ||
NM_006909.3:c.2907-29_2907-23del MANE Select | NP_008840.1:n.2907-29_2907-23del |