HGVS | Genome Assembly |
---|---|
NC_000014.9:g.76371434C= , CM000676.2:g.76371434C= | GRCh38 |
NC_000014.8:g.76837777C= , CM000676.1:g.76837777C= | GRCh37 |
NC_000014.7:g.75907530C= | NCBI36 |
NG_012278.1:g.5088C= | |
NG_012278.2:g.5088C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000380887.7:c.-284C= | ENSP00000370270.2:n.-284C= | |
ENST00000505752.6:c.-284C= | ENSP00000423004.1:n.-284C= | |
ENST00000512784.6:c.2+60518C= | ENSP00000424992.2:n.2+60518C= | |
ENST00000505752.5:c.-284C= | ENSP00000423004.1:n.-284C= | |
ENST00000512784.5:c.2+60518C= | ENSP00000424992.1:n.2+60518C= | |
NM_004452.3:c.-284C= | NP_004443.3:n.-284C= | |
XM_011536548.1:c.-284C= | XP_011534850.1:n.-284C= | |
NM_004452.4:c.-284C= | NP_004443.3:n.-284C= |