HGVS | Genome Assembly |
---|---|
NC_000015.10:g.48411065G>C , CM000677.2:g.48411065G>C | GRCh38 |
NC_000015.9:g.48703262G>C , CM000677.1:g.48703262G>C | GRCh37 |
NC_000015.8:g.46490554G>C | NCBI36 |
NG_008805.2:g.239724C>G , LRG_778:g.239724C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000559133.6:c.*1349C>G | ENSP00000453958.2:n.*1349C>G | |
ENST00000682158.1:n.1922C>G | ||
ENST00000682170.1:n.2722C>G | ||
ENST00000682767.1:n.1838C>G | ||
ENST00000316623.10:c.8541C>G MANE Select | ENSP00000325527.5:p.Asp2847Glu | |
ENST00000316623.9:c.8541C>G | ENSP00000325527.5:p.Asp2847Glu | |
ENST00000559133.5:c.3910C>G | ||
NM_000138.4:c.8541C>G , LRG_778t1:c.8541C>G | NP_000129.3:p.Asp2847Glu | |
NM_000138.5:c.8541C>G MANE Select | NP_000129.3:p.Asp2847Glu |