HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94775487C= , CM000672.2:g.94775487C= | GRCh38 |
NC_000010.10:g.96535244C= , CM000672.1:g.96535244C= | GRCh37 |
NC_000010.9:g.96525234C= | NCBI36 |
NG_008384.2:g.17782C= | |
NG_008384.3:g.17807C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371321.9:c.429C= MANE Select | ENSP00000360372.3:p.Asp143= | |
ENST00000645461.1:n.1482C= | ||
ENST00000371321.7:c.429C= | ENSP00000360372.3:p.Asp143= | |
ENST00000464755.1:c.1192C= | ENSP00000483243.1:n.1192C= | |
ENST00000480405.2:c.429C= | ENSP00000483847.1:p.Asp143= | |
NM_000769.2:c.429C= | NP_000760.1:p.Asp143= | |
NM_000769.4:c.429C= MANE Select | NP_000760.1:p.Asp143= |