HGVS | Genome Assembly |
---|---|
NC_000019.10:g.1401371T>C , CM000681.2:g.1401371T>C | GRCh38 |
NC_000019.9:g.1401370T>C , CM000681.1:g.1401370T>C | GRCh37 |
NC_000019.8:g.1352370T>C | NCBI36 |
NG_009785.1:g.5183A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252288.8:c.106A>G MANE Select | ENSP00000252288.1:p.Ile36Val | |
ENST00000447102.8:c.106A>G | ENSP00000403536.2:p.Ile36Val | |
ENST00000640762.1:c.106A>G | ENSP00000492031.1:p.Ile36Val | |
ENST00000252288.6:c.106A>G | ENSP00000252288.1:p.Ile36Val | |
ENST00000447102.7:c.106A>G | ENSP00000403536.2:p.Ile36Val | |
NM_000156.5:c.106A>G | NP_000147.1:p.Ile36Val | |
NM_138924.2:c.106A>G | NP_620279.1:p.Ile36Val | |
NM_000156.6:c.106A>G MANE Select | NP_000147.1:p.Ile36Val | |
NM_138924.3:c.106A>G | NP_620279.1:p.Ile36Val |