HGVS | Genome Assembly |
---|---|
NC_000006.12:g.160553481G= , CM000668.2:g.160553481G= | GRCh38 |
NC_000006.11:g.160974513G= , CM000668.1:g.160974513G= | GRCh37 |
NC_000006.10:g.160894503G= | NCBI36 |
NG_016147.1:g.117895C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000316300.10:c.4973+2544C= MANE Select | ENSP00000321334.6:n.4973+2544C= | |
ENST00000316300.9:c.4973+2544C= | ENSP00000321334.5:n.4973+2544C= | |
NM_005577.2:c.4973+2544C= | NP_005568.2:n.4973+2544C= | |
NM_005577.3:c.4973+2544C= | NP_005568.2:n.4973+2544C= | |
NM_005577.4:c.4973+2544C= MANE Select | NP_005568.2:n.4973+2544C= |