HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1428111C= , CM000667.2:g.1428111C= | GRCh38 |
NC_000005.9:g.1428226C= , CM000667.1:g.1428226C= | GRCh37 |
NC_000005.8:g.1481226C= | NCBI36 |
NG_015885.1:g.22318G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270349.12:c.653+4353G= MANE Select | ENSP00000270349.9:n.653+4353G= | |
ENST00000270349.11:c.653+4353G= | ENSP00000270349.9:n.653+4353G= | |
NM_001044.4:c.653+4353G= | NP_001035.1:n.653+4353G= | |
NM_001044.5:c.653+4353G= MANE Select | NP_001035.1:n.653+4353G= |