HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94852966C= , CM000672.2:g.94852966C= | GRCh38 |
NC_000010.10:g.96612723C= , CM000672.1:g.96612723C= | GRCh37 |
NC_000010.9:g.96602713C= | NCBI36 |
NG_008384.2:g.95261C= | |
NG_008384.3:g.95286C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371321.9:c.*52C= MANE Select | ENSP00000360372.3:n.*52C= | |
ENST00000645461.1:n.2436C= | ||
ENST00000371321.7:c.*52C= | ENSP00000360372.3:n.*52C= | |
ENST00000464755.1:c.2288C= | ENSP00000483243.1:n.2288C= | |
NM_000769.2:c.*52C= | NP_000760.1:n.*52C= | |
NM_000769.4:c.*52C= MANE Select | NP_000760.1:n.*52C= |