HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52492669A= , CM000674.2:g.52492669A= | GRCh38 |
NC_000012.11:g.52886453A= , CM000674.1:g.52886453A= | GRCh37 |
NC_000012.10:g.51172720A= | NCBI36 |
NG_008298.1:g.5729T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000330722.7:c.520T= MANE Select | ENSP00000369317.3:p.Phe174= | |
ENST00000330722.6:c.520T= | ENSP00000369317.3:p.Phe174= | |
ENST00000549898.5:n.41T= | ||
NM_005554.3:c.520T= | NP_005545.1:p.Phe174= | |
NM_005554.4:c.520T= MANE Select | NP_005545.1:p.Phe174= |