HGVS | Genome Assembly |
---|---|
NC_000004.12:g.52038297T= , CM000666.2:g.52038297T= | GRCh38 |
NC_000004.11:g.52904463T= , CM000666.1:g.52904463T= | GRCh37 |
NC_000004.10:g.52599220T= | NCBI36 |
NG_008891.1:g.5023A= , LRG_204:g.5023A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000381431.10:c.-38A= MANE Select | ENSP00000370839.6:n.-38A= | |
ENST00000381431.9:c.-38A= | ENSP00000370839.5:n.-38A= | |
NM_000232.4:c.-38A= , LRG_204t1:c.-38A= | NP_000223.1:n.-38A= | |
XM_011534403.1:c.-38A= | XP_011532705.1:n.-38A= | |
NM_000232.5:c.-38A= MANE Select | NP_000223.1:n.-38A= |