HGVS | Genome Assembly |
---|---|
NC_000012.12:g.57764094T>C , CM000674.2:g.57764094T>C | GRCh38 |
NC_000012.11:g.58157877T>C , CM000674.1:g.58157877T>C | GRCh37 |
NC_000012.10:g.56444144T>C | NCBI36 |
NG_007076.1:g.8100A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000713544.1:c.1296+4A>G | ENSP00000518840.1:n.1296+4A>G | |
ENST00000713545.1:c.*220+4A>G | ENSP00000518841.1:n.*220+4A>G | |
ENST00000228606.9:c.1215+4A>G MANE Select | ENSP00000228606.4:n.1215+4A>G | |
ENST00000228606.8:c.1215+4A>G | ENSP00000228606.4:n.1215+4A>G | |
ENST00000547344.5:n.1354+4A>G | ||
NM_000785.3:c.1215+4A>G | NP_000776.1:n.1215+4A>G | |
NM_000785.4:c.1215+4A>G MANE Select | NP_000776.1:n.1215+4A>G |