HGVS | Genome Assembly |
---|---|
NC_000007.14:g.147132487G= , CM000669.2:g.147132487G= | GRCh38 |
NC_000007.13:g.146829579G= , CM000669.1:g.146829579G= | GRCh37 |
NC_000007.12:g.146460512G= | NCBI36 |
NG_007092.2:g.1021127G= | |
NG_007092.3:g.1021487G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361727.8:c.1326G= MANE Select | ENSP00000354778.3:p.Met442= | |
ENST00000636561.1:n.1229G= | ||
ENST00000636870.1:n.1188G= | ||
ENST00000637150.1:n.1255G= | ||
ENST00000637694.1:n.1229G= | ||
ENST00000637825.1:n.809G= | ||
ENST00000638117.1:n.1229G= | ||
ENST00000361727.7:c.1326G= | ENSP00000354778.3:p.Met442= | |
NM_014141.5:c.1326G= | NP_054860.1:p.Met442= | |
XM_017011950.2:c.1326G= | XP_016867439.1:p.Met442= | |
NM_014141.6:c.1326G= MANE Select | NP_054860.1:p.Met442= |