HGVS | Genome Assembly |
---|---|
NC_000005.10:g.111072495C>G , CM000667.2:g.111072495C>G | GRCh38 |
NC_000005.9:g.110408193C>G , CM000667.1:g.110408193C>G | GRCh37 |
NC_000005.8:g.110436092C>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344895.4:c.172-393C>G MANE Select | ENSP00000339804.3:n.172-393C>G | |
ENST00000344895.3:c.172-393C>G | ENSP00000339804.3:n.172-393C>G | |
ENST00000420978.6:c.172-393C>G | ENSP00000399099.2:n.172-393C>G | |
NM_033035.4:c.172-393C>G | NP_149024.1:n.172-393C>G | |
NR_045089.1:n.1576-393C>G | ||
NM_033035.5:c.172-393C>G MANE Select | NP_149024.1:n.172-393C>G | |
NR_045089.2:n.1594-393C>G |