HGVS | Genome Assembly |
---|---|
NC_000007.14:g.117479302A= , CM000669.2:g.117479302A= | GRCh38 |
NC_000007.13:g.117119356A= , CM000669.1:g.117119356A= | GRCh37 |
NC_000007.12:g.116906592A= | NCBI36 |
NG_016465.4:g.18519A= , LRG_663:g.18519A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000446805.2:c.-467A= | ENSP00000417012.1:n.-467A= | |
ENST00000673785.1:c.-406+13471A= | ENSP00000501235.1:n.-406+13471A= | |
ENST00000546407.1:n.166+3494A= | ||
XM_011515751.1:c.100A= | XP_011514053.1:p.Ile34= | |
XM_011515752.1:c.100A= | XP_011514054.1:p.Ile34= | |
XM_011515754.1:c.-795A= | XP_011514056.1:n.-795A= |