HGVS | Genome Assembly |
---|---|
NC_000005.10:g.81207031T>A , CM000667.2:g.81207031T>A | GRCh38 |
NC_000005.9:g.80502850T>A , CM000667.1:g.80502850T>A | GRCh37 |
NC_000005.8:g.80538606T>A | NCBI36 |
NG_030334.1:g.251343T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000265080.9:c.2967+126T>A MANE Select | ENSP00000265080.4:n.2967+126T>A | |
ENST00000265080.8:c.2967+126T>A | ENSP00000265080.4:n.2967+126T>A | |
ENST00000503795.1:c.2967+126T>A | ENSP00000421771.1:n.2967+126T>A | |
NM_006909.2:c.2967+126T>A | NP_008840.1:n.2967+126T>A | |
XM_017009682.2:c.2682+126T>A | XP_016865171.1:n.2682+126T>A | |
XR_002956166.1:n.3083+126T>A | ||
NM_006909.3:c.2967+126T>A MANE Select | NP_008840.1:n.2967+126T>A |