HGVS | Genome Assembly |
---|---|
NC_000005.10:g.81206981C>G , CM000667.2:g.81206981C>G | GRCh38 |
NC_000005.9:g.80502800C>G , CM000667.1:g.80502800C>G | GRCh37 |
NC_000005.8:g.80538556C>G | NCBI36 |
NG_030334.1:g.251293C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000265080.9:c.2967+76C>G MANE Select | ENSP00000265080.4:n.2967+76C>G | |
ENST00000265080.8:c.2967+76C>G | ENSP00000265080.4:n.2967+76C>G | |
ENST00000503795.1:c.2967+76C>G | ENSP00000421771.1:n.2967+76C>G | |
NM_006909.2:c.2967+76C>G | NP_008840.1:n.2967+76C>G | |
XM_017009682.2:c.2682+76C>G | XP_016865171.1:n.2682+76C>G | |
XR_002956166.1:n.3083+76C>G | ||
NM_006909.3:c.2967+76C>G MANE Select | NP_008840.1:n.2967+76C>G |