HGVS | Genome Assembly |
---|---|
NC_000014.9:g.60649457C= , CM000676.2:g.60649457C= | GRCh38 |
NC_000014.8:g.61116175C= , CM000676.1:g.61116175C= | GRCh37 |
NC_000014.7:g.60185928C= | NCBI36 |
NG_008231.1:g.4981G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000645694.3:c.-268G= MANE Select | ENSP00000494686.1:n.-268G= | |
ENST00000247182.6:c.-268G= | ENSP00000247182.5:n.-268G= | |
ENST00000553535.2:n.248+2478G= | ||
ENST00000554986.2:c.42-2880G= | ENSP00000452700.2:n.42-2880G= | |
ENST00000555955.3:n.1197+2478G= | ||
XM_017021602.2:c.-268G= | XP_016877091.1:n.-268G= | |
NM_005982.4:c.-268G= MANE Select | NP_005973.1:n.-268G= |