HGVS | Genome Assembly |
---|---|
NC_000006.12:g.131851148T= , CM000668.2:g.131851148T= | GRCh38 |
NC_000006.11:g.132172288T= , CM000668.1:g.132172288T= | GRCh37 |
NC_000006.10:g.132213981T= | NCBI36 |
NG_008206.1:g.48133T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000647893.1:c.437T= MANE Select | ENSP00000498074.1:p.Ile146= | |
ENST00000650147.1:c.115T= | ||
ENST00000650437.1:c.108+1042T= | ||
ENST00000360971.6:c.437T= | ENSP00000354238.2:p.Ile146= | |
ENST00000486853.1:n.457T= | ||
ENST00000513998.5:c.437T= | ENSP00000422424.1:p.Ile146= | |
NM_006208.2:c.437T= | NP_006199.2:p.Ile146= | |
NM_006208.3:c.437T= MANE Select | NP_006199.2:p.Ile146= |