HGVS | Genome Assembly |
---|---|
NC_000008.11:g.10622781T= , CM000670.2:g.10622781T= | GRCh38 |
NC_000008.10:g.10480291T= , CM000670.1:g.10480291T= | GRCh37 |
NC_000008.9:g.10517701T= | NCBI36 |
NG_028035.1:g.37327A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382483.4:c.421A= MANE Select | ENSP00000371923.3:p.Thr141= | |
ENST00000329335.3:n.671A= | ||
ENST00000382483.3:c.421A= | ENSP00000371923.3:p.Thr141= | |
NM_178857.5:c.421A= | NP_849188.4:p.Thr141= | |
NM_178857.6:c.421A= MANE Select | NP_849188.4:p.Thr141= |