HGVS | Genome Assembly |
---|---|
NC_000001.11:g.168293309_168293310insAG , CM000663.2:g.168293309_168293310insAG | GRCh38 |
NC_000001.10:g.168262547_168262548insAG , CM000663.1:g.168262547_168262548insAG | GRCh37 |
NC_000001.9:g.166529171_166529172insAG | NCBI36 |
NG_008244.1:g.17270_17271insAG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367821.8:c.603+31_603+32insAG MANE Select | ENSP00000356795.3:n.603+31_603+32insAG | |
ENST00000367821.7:c.603+31_603+32insAG | ENSP00000356795.3:n.603+31_603+32insAG | |
ENST00000431969.5:c.400+31_400+32insAG | ||
NM_005149.2:c.603+31_603+32insAG | NP_005140.1:n.603+31_603+32insAG | |
NM_005149.3:c.603+31_603+32insAG MANE Select | NP_005140.1:n.603+31_603+32insAG |