HGVS | Genome Assembly |
---|---|
NC_000003.12:g.10141847A= , CM000665.2:g.10141847A= | GRCh38 |
NC_000003.11:g.10183531A= , CM000665.1:g.10183531A= | GRCh37 |
NC_000003.10:g.10158531A= | NCBI36 |
NG_008212.3:g.5213A= , LRG_322:g.5213A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000696142.1:c.-1A= | ENSP00000512434.1:n.-1A= | |
ENST00000696153.1:c.-1A= | ENSP00000512444.1:n.-1A= | |
ENST00000256474.3:c.-1A= MANE Select | ENSP00000256474.3:n.-1A= | |
ENST00000256474.2:c.-1A= | ENSP00000256474.2:n.-1A= | |
ENST00000345392.2:c.-1A= | ENSP00000344757.2:n.-1A= | |
NM_000551.3:c.-1A= , LRG_322t1:c.-1A= | NP_000542.1:n.-1A= | |
NM_198156.2:c.-1A= | NP_937799.1:n.-1A= | |
XM_011534078.1:c.-1A= | XP_011532380.1:n.-1A= | |
NM_001354723.1:c.-1A= | NP_001341652.1:n.-1A= | |
NM_000551.4:c.-1A= MANE Select | NP_000542.1:n.-1A= | |
NM_001354723.2:c.-1A= | NP_001341652.1:n.-1A= | |
NM_198156.3:c.-1A= | NP_937799.1:n.-1A= |