HGVS | Genome Assembly |
---|---|
NC_000008.11:g.64624575A= , CM000670.2:g.64624575A= | GRCh38 |
NC_000008.10:g.65537132A= , CM000670.1:g.65537132A= | GRCh37 |
NC_000008.9:g.65699686A= | NCBI36 |
NG_008338.1:g.179217T= | |
NG_008338.2:g.179217T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000310193.4:c.123-36T= MANE Select | ENSP00000310721.3:n.123-36T= | |
ENST00000310193.3:c.123-36T= | ENSP00000310721.3:n.123-36T= | |
NM_004820.3:c.123-36T= | NP_004811.1:n.123-36T= | |
NM_001324112.1:c.123-36T= | NP_001311041.1:n.123-36T= | |
NM_004820.4:c.123-36T= | NP_004811.1:n.123-36T= | |
XM_017014002.1:c.189-36T= | XP_016869491.1:n.189-36T= | |
NM_004820.5:c.123-36T= MANE Select | NP_004811.1:n.123-36T= | |
NM_001324112.2:c.123-36T= | NP_001311041.1:n.123-36T= |