HGVS | Genome Assembly |
---|---|
NC_000007.14:g.94426023C= , CM000669.2:g.94426023C= | GRCh38 |
NC_000007.13:g.94055335C= , CM000669.1:g.94055335C= | GRCh37 |
NC_000007.12:g.93893271C= | NCBI36 |
NG_007405.1:g.36463C= , LRG_2:g.36463C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000297268.11:c.2969C= MANE Select | ENSP00000297268.6:p.Ala990= | |
ENST00000297268.10:c.2969C= | ENSP00000297268.6:p.Ala990= | |
ENST00000478215.1:n.528C= | ||
ENST00000481570.5:n.2942C= | ||
ENST00000620463.1:c.2963C= | ENSP00000477719.1:p.Ala988= | |
NM_000089.3:c.2969C= , LRG_2t1:c.2969C= | NP_000080.2:p.Ala990= | |
NM_000089.4:c.2969C= MANE Select | NP_000080.2:p.Ala990= |