HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52488007T= , CM000674.2:g.52488007T= | GRCh38 |
NC_000012.11:g.52881791T= , CM000674.1:g.52881791T= | GRCh37 |
NC_000012.10:g.51168058T= | NCBI36 |
NG_008298.1:g.10391A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000330722.7:c.1460-52A= MANE Select | ENSP00000369317.3:n.1460-52A= | |
ENST00000330722.6:c.1460-52A= | ENSP00000369317.3:n.1460-52A= | |
NM_005554.3:c.1460-52A= | NP_005545.1:n.1460-52A= | |
NM_005554.4:c.1460-52A= MANE Select | NP_005545.1:n.1460-52A= |