HGVS | Genome Assembly |
---|---|
NC_000006.12:g.143485108_143485109delinsTG , CM000668.2:g.143485108_143485109delinsTG | GRCh38 |
NC_000006.11:g.143806245_143806246delinsTG , CM000668.1:g.143806245_143806246delinsTG | GRCh37 |
NC_000006.10:g.143847938_143847939delinsTG | NCBI36 |
NG_008459.1:g.39328_39329delinsTG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367591.5:c.942-44_942-43delinsTG MANE Select | ENSP00000356563.4:n.942-44_942-43delinsTG | |
ENST00000367591.4:c.942-44_942-43delinsTG | ENSP00000356563.4:n.942-44_942-43delinsTG | |
ENST00000585848.1:n.37_38delinsTG | ||
NM_003630.2:c.942-44_942-43delinsTG | NP_003621.1:n.942-44_942-43delinsTG | |
NM_003630.3:c.942-44_942-43delinsTG MANE Select | NP_003621.1:n.942-44_942-43delinsTG |