HGVS | Genome Assembly |
---|---|
NC_000007.14:g.94415268A>G , CM000669.2:g.94415268A>G | GRCh38 |
NC_000007.13:g.94044580A>G , CM000669.1:g.94044580A>G | GRCh37 |
NC_000007.12:g.93882516A>G | NCBI36 |
NG_007405.1:g.25708A>G , LRG_2:g.25708A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000297268.11:c.1762A>G MANE Select | ENSP00000297268.6:p.Arg588Gly | |
ENST00000297268.10:c.1762A>G | ENSP00000297268.6:p.Arg588Gly | |
ENST00000473573.5:n.99A>G | ||
ENST00000488298.5:n.186A>G | ||
ENST00000620463.1:c.1756A>G | ENSP00000477719.1:p.Arg586Gly | |
NM_000089.3:c.1762A>G , LRG_2t1:c.1762A>G | NP_000080.2:p.Arg588Gly | |
NM_000089.4:c.1762A>G MANE Select | NP_000080.2:p.Arg588Gly |