HGVS | Genome Assembly |
---|---|
NC_000001.11:g.168293354_168293355insG , CM000663.2:g.168293354_168293355insG | GRCh38 |
NC_000001.10:g.168262592_168262593insG , CM000663.1:g.168262592_168262593insG | GRCh37 |
NC_000001.9:g.166529216_166529217insG | NCBI36 |
NG_008244.1:g.17315_17316insG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367821.8:c.603+76_603+77insG MANE Select | ENSP00000356795.3:n.603+76_603+77insG | |
ENST00000367821.7:c.603+76_603+77insG | ENSP00000356795.3:n.603+76_603+77insG | |
ENST00000431969.5:c.400+76_400+77insG | ||
NM_005149.2:c.603+76_603+77insG | NP_005140.1:n.603+76_603+77insG | |
NM_005149.3:c.603+76_603+77insG MANE Select | NP_005140.1:n.603+76_603+77insG |