HGVS | Genome Assembly |
---|---|
NC_000007.14:g.94404535A= , CM000669.2:g.94404535A= | GRCh38 |
NC_000007.13:g.94033847A= , CM000669.1:g.94033847A= | GRCh37 |
NC_000007.12:g.93871783A= | NCBI36 |
NG_007405.1:g.14975A= , LRG_2:g.14975A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000297268.11:c.280-21A= MANE Select | ENSP00000297268.6:n.280-21A= | |
ENST00000297268.10:c.280-21A= | ENSP00000297268.6:n.280-21A= | |
ENST00000620463.1:c.274-21A= | ENSP00000477719.1:n.274-21A= | |
NM_000089.3:c.280-21A= , LRG_2t1:c.280-21A= | NP_000080.2:n.280-21A= | |
NM_000089.4:c.280-21A= MANE Select | NP_000080.2:n.280-21A= |