HGVS | Genome Assembly |
---|---|
NC_000005.10:g.81206725T>A , CM000667.2:g.81206725T>A | GRCh38 |
NC_000005.9:g.80502544T>A , CM000667.1:g.80502544T>A | GRCh37 |
NC_000005.8:g.80538300T>A | NCBI36 |
NG_030334.1:g.251037T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000265080.9:c.2907-120T>A MANE Select | ENSP00000265080.4:n.2907-120T>A | |
ENST00000265080.8:c.2907-120T>A | ENSP00000265080.4:n.2907-120T>A | |
ENST00000503795.1:c.2907-120T>A | ENSP00000421771.1:n.2907-120T>A | |
NM_006909.2:c.2907-120T>A | NP_008840.1:n.2907-120T>A | |
XM_017009682.2:c.2622-120T>A | XP_016865171.1:n.2622-120T>A | |
XR_002956166.1:n.3023-120T>A | ||
NM_006909.3:c.2907-120T>A MANE Select | NP_008840.1:n.2907-120T>A |