HGVS | Genome Assembly |
---|---|
NC_000003.12:g.30606592G= , CM000665.2:g.30606592G= | GRCh38 |
NC_000003.11:g.30648084G= , CM000665.1:g.30648084G= | GRCh37 |
NC_000003.10:g.30623088G= | NCBI36 |
NG_007490.1:g.5091G= , LRG_779:g.5091G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000295754.9:c.-292G= | ENSP00000295754.5:n.-292G= | |
NM_001024847.2:c.-292G= , LRG_779t1:c.-292G= | NP_001020018.1:n.-292G= | |
NM_003242.5:c.-292G= | NP_003233.4:n.-292G= | |
XM_011534045.1:c.-13G= | XP_011532347.1:n.-13G= | |
XM_011534045.3:c.-13G= | XP_011532347.1:n.-13G= |