HGVS | Genome Assembly |
---|---|
NC_000009.12:g.93953746A>C , CM000671.2:g.93953746A>C | GRCh38 |
NC_000009.11:g.96716028A>C , CM000671.1:g.96716028A>C | GRCh37 |
NC_000009.10:g.95755849A>C | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000253968.11:c.224-559T>G MANE Select | ENSP00000253968.5:n.224-559T>G | |
ENST00000253968.10:c.224-559T>G | ENSP00000253968.5:n.224-559T>G | |
NM_021570.3:c.224-559T>G | NP_067545.3:n.224-559T>G | |
NM_021570.4:c.224-559T>G MANE Select | NP_067545.3:n.224-559T>G |