HGVS | Genome Assembly |
---|---|
NC_000010.11:g.119672141G= , CM000672.2:g.119672141G= | GRCh38 |
NC_000010.10:g.121431653G= , CM000672.1:g.121431653G= | GRCh37 |
NC_000010.9:g.121421643G= | NCBI36 |
NG_016125.1:g.25772G= , LRG_742:g.25772G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369085.8:c.508-114G= MANE Select | ENSP00000358081.4:n.508-114G= | |
ENST00000369085.7:c.508-114G= | ENSP00000358081.3:n.508-114G= | |
ENST00000450186.1:c.334-114G= | ENSP00000410036.1:n.334-114G= | |
NM_004281.3:c.508-114G= , LRG_742t1:c.508-114G= | NP_004272.2:n.508-114G= | |
XM_005270287.1:c.508-114G= | XP_005270344.1:n.508-114G= | |
XM_005270287.2:c.508-114G= | XP_005270344.1:n.508-114G= | |
NM_004281.4:c.508-114G= MANE Select | NP_004272.2:n.508-114G= |