HGVS | Genome Assembly |
---|---|
NC_000012.12:g.57764646A>C , CM000674.2:g.57764646A>C | GRCh38 |
NC_000012.11:g.58158429A>C , CM000674.1:g.58158429A>C | GRCh37 |
NC_000012.10:g.56444696A>C | NCBI36 |
NG_007076.1:g.7548T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000713544.1:c.1045-96T>G | ENSP00000518840.1:n.1045-96T>G | |
ENST00000713545.1:c.1022-96T>G | ENSP00000518841.1:n.1022-96T>G | |
ENST00000228606.9:c.964-96T>G MANE Select | ENSP00000228606.4:n.964-96T>G | |
ENST00000228606.8:c.964-96T>G | ENSP00000228606.4:n.964-96T>G | |
ENST00000546567.5:c.259-96T>G | ENSP00000449472.1:n.259-96T>G | |
ENST00000547344.5:n.1103-96T>G | ||
ENST00000547451.1:n.871T>G | ||
NM_000785.3:c.964-96T>G | NP_000776.1:n.964-96T>G | |
NM_000785.4:c.964-96T>G MANE Select | NP_000776.1:n.964-96T>G |