HGVS | Genome Assembly |
---|---|
NC_000010.11:g.119669707G= , CM000672.2:g.119669707G= | GRCh38 |
NC_000010.10:g.121429219G= , CM000672.1:g.121429219G= | GRCh37 |
NC_000010.9:g.121419209G= | NCBI36 |
NG_016125.1:g.23338G= , LRG_742:g.23338G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369085.8:c.181-144G= MANE Select | ENSP00000358081.4:n.181-144G= | |
ENST00000369085.7:c.181-144G= | ENSP00000358081.3:n.181-144G= | |
ENST00000450186.1:c.7-144G= | ENSP00000410036.1:n.7-144G= | |
NM_004281.3:c.181-144G= , LRG_742t1:c.181-144G= | NP_004272.2:n.181-144G= | |
XM_005270287.1:c.181-144G= | XP_005270344.1:n.181-144G= | |
XM_005270287.2:c.181-144G= | XP_005270344.1:n.181-144G= | |
NM_004281.4:c.181-144G= MANE Select | NP_004272.2:n.181-144G= |