HGVS | Genome Assembly |
---|---|
NC_000004.12:g.99420687A= , CM000666.2:g.99420687A= | GRCh38 |
NC_000004.11:g.100341844A= , CM000666.1:g.100341844A= | GRCh37 |
NC_000004.10:g.100560867A= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000437033.7:c.671T= MANE Select | ENSP00000414254.2:p.Leu224= | |
ENST00000209665.8:c.707T= | ENSP00000209665.4:p.Leu236= | |
ENST00000437033.6:c.671T= | ENSP00000414254.2:p.Leu224= | |
ENST00000476959.5:c.731T= | ENSP00000420269.1:p.Leu244= | |
ENST00000482593.5:c.500T= | ENSP00000420613.1:p.Leu167= | |
NM_000673.4:c.707T= | NP_000664.2:p.Leu236= | |
NM_001166504.1:c.731T= | NP_001159976.1:p.Leu244= | |
NM_000673.7:c.671T= MANE Select | NP_000664.3:p.Leu224= | |
NM_001166504.2:c.731T= | NP_001159976.1:p.Leu244= |