HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52492471C= , CM000674.2:g.52492471C= | GRCh38 |
NC_000012.11:g.52886255C= , CM000674.1:g.52886255C= | GRCh37 |
NC_000012.10:g.51172522C= | NCBI36 |
NG_008298.1:g.5927G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000330722.7:c.540+178G= MANE Select | ENSP00000369317.3:n.540+178G= | |
ENST00000330722.6:c.540+178G= | ENSP00000369317.3:n.540+178G= | |
ENST00000549898.5:n.61+178G= | ||
NM_005554.3:c.540+178G= | NP_005545.1:n.540+178G= | |
NM_005554.4:c.540+178G= MANE Select | NP_005545.1:n.540+178G= |