HGVS | Genome Assembly |
---|---|
NC_000001.11:g.26419836A>G , CM000663.2:g.26419836A>G | GRCh38 |
NC_000001.10:g.26746327A>G , CM000663.1:g.26746327A>G | GRCh37 |
NC_000001.9:g.26618914A>G | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000326279.11:c.229-5467A>G MANE Select | ENSP00000363314.3:n.229-5467A>G | |
ENST00000254231.4:c.229-5467A>G | ENSP00000254231.4:n.229-5467A>G | |
ENST00000326279.10:c.229-5467A>G | ENSP00000363314.3:n.229-5467A>G | |
NM_024674.4:c.229-5467A>G | NP_078950.1:n.229-5467A>G | |
NM_024674.5:c.229-5467A>G | NP_078950.1:n.229-5467A>G | |
XM_011542148.1:c.229-5467A>G | XP_011540450.1:n.229-5467A>G | |
XM_011542148.2:c.229-5467A>G | XP_011540450.1:n.229-5467A>G | |
NM_024674.6:c.229-5467A>G MANE Select | NP_078950.1:n.229-5467A>G |