HGVS | Genome Assembly |
---|---|
NC_000008.11:g.118947604_118947605delinsTA , CM000670.2:g.118947604_118947605delinsTA | GRCh38 |
NC_000008.10:g.119959843_119959844delinsTA , CM000670.1:g.119959843_119959844delinsTA | GRCh37 |
NC_000008.9:g.120029024_120029025delinsTA | NCBI36 |
NG_012202.1:g.9540_9541delinsTA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000297350.9:c.30+4187_30+4188delinsTA MANE Select | ENSP00000297350.4:n.30+4187_30+4188delins... | |
ENST00000297350.8:c.30+4187_30+4188delinsTA | ENSP00000297350.4:n.30+4187_30+4188delins... | |
ENST00000517352.1:c.30+4187_30+4188delinsTA | ENSP00000427924.1:n.30+4187_30+4188delins... | |
NM_002546.3:c.30+4187_30+4188delinsTA | NP_002537.3:n.30+4187_30+4188delinsTA | |
NM_002546.4:c.30+4187_30+4188delinsTA MANE Select | NP_002537.3:n.30+4187_30+4188delinsTA |