HGVS | Genome Assembly |
---|---|
NC_000001.11:g.169549619T= , CM000663.2:g.169549619T= | GRCh38 |
NC_000001.10:g.169518857T= , CM000663.1:g.169518857T= | GRCh37 |
NC_000001.9:g.167785481T= | NCBI36 |
NG_011806.1:g.41913A= , LRG_553:g.41913A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367797.9:c.1611+182A= MANE Select | ENSP00000356771.3:n.1611+182A= | |
ENST00000367796.3:c.1611+182A= | ENSP00000356770.3:n.1611+182A= | |
ENST00000367797.7:c.1611+182A= | ENSP00000356771.3:n.1611+182A= | |
NM_000130.4:c.1611+182A= , LRG_553t1:c.1611+182A= | NP_000121.2:n.1611+182A= | |
XM_017000660.2:c.1200+182A= | XP_016856149.1:n.1200+182A= | |
NM_000130.5:c.1611+182A= MANE Select | NP_000121.2:n.1611+182A= |