HGVS | Genome Assembly |
---|---|
NC_000007.14:g.147492644C= , CM000669.2:g.147492644C= | GRCh38 |
NC_000007.13:g.147189736C= , CM000669.1:g.147189736C= | GRCh37 |
NC_000007.12:g.146820669C= | NCBI36 |
NG_007092.2:g.1381284C= | |
NG_007092.3:g.1381644C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361727.8:c.1777+6603C= MANE Select | ENSP00000354778.3:n.1777+6603C= | |
ENST00000636870.1:n.1639+6603C= | ||
ENST00000637694.1:n.1681-3977C= | ||
ENST00000637825.1:n.1260+6603C= | ||
ENST00000638117.1:n.1680+6603C= | ||
ENST00000361727.7:c.1777+6603C= | ENSP00000354778.3:n.1777+6603C= | |
NM_014141.5:c.1777+6603C= | NP_054860.1:n.1777+6603C= | |
XM_006715919.1:c.265+6603C= | XP_006715982.1:n.265+6603C= | |
XM_017011950.2:c.1777+6603C= | XP_016867439.1:n.1777+6603C= | |
NM_014141.6:c.1777+6603C= MANE Select | NP_054860.1:n.1777+6603C= |