HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52488073G= , CM000674.2:g.52488073G= | GRCh38 |
NC_000012.11:g.52881857G= , CM000674.1:g.52881857G= | GRCh37 |
NC_000012.10:g.51168124G= | NCBI36 |
NG_008298.1:g.10325C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000330722.7:c.1455C= MANE Select | ENSP00000369317.3:p.Asn485= | |
ENST00000330722.6:c.1455C= | ENSP00000369317.3:p.Asn485= | |
NM_005554.3:c.1455C= | NP_005545.1:p.Asn485= | |
NM_005554.4:c.1455C= MANE Select | NP_005545.1:p.Asn485= |