HGVS | Genome Assembly |
---|---|
NC_000007.14:g.94404667A>G , CM000669.2:g.94404667A>G | GRCh38 |
NC_000007.13:g.94033979A>G , CM000669.1:g.94033979A>G | GRCh37 |
NC_000007.12:g.93871915A>G | NCBI36 |
NG_007405.1:g.15107A>G , LRG_2:g.15107A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000297268.11:c.325-26A>G MANE Select | ENSP00000297268.6:n.325-26A>G | |
ENST00000297268.10:c.325-26A>G | ENSP00000297268.6:n.325-26A>G | |
ENST00000620463.1:c.319-26A>G | ENSP00000477719.1:n.319-26A>G | |
NM_000089.3:c.325-26A>G , LRG_2t1:c.325-26A>G | NP_000080.2:n.325-26A>G | |
NM_000089.4:c.325-26A>G MANE Select | NP_000080.2:n.325-26A>G |