HGVS | Genome Assembly |
---|---|
NC_000019.10:g.40848431T>C , CM000681.2:g.40848431T>C | GRCh38 |
NC_000019.9:g.41354336T>C , CM000681.1:g.41354336T>C | GRCh37 |
NC_000019.8:g.46046176T>C | NCBI36 |
NG_008377.1:g.7017A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000301141.10:c.494-52A>G MANE Select | ENSP00000301141.4:n.494-52A>G | |
ENST00000301141.9:c.494-52A>G | ENSP00000301141.4:n.494-52A>G | |
ENST00000596719.5:n.345-52A>G | ||
ENST00000600495.1:c.*306-52A>G | ENSP00000472905.1:n.*306-52A>G | |
ENST00000601627.1:c.120-43560T>C | ||
ENST00000610301.1:c.494-52A>G | ENSP00000477899.1:n.494-52A>G | |
NM_000762.5:c.494-52A>G | NP_000753.3:n.494-52A>G | |
NM_000762.6:c.494-52A>G MANE Select | NP_000753.3:n.494-52A>G |