HGVS | Genome Assembly |
---|---|
NC_000002.12:g.135856609_135856611delinsCCT , CM000664.2:g.135856609_135856611delinsCCT | GRCh38 |
NC_000002.11:g.136614179_136614181delinsCCT , CM000664.1:g.136614179_136614181delinsCCT | GRCh37 |
NC_000002.10:g.136330649_136330651delinsCCT | NCBI36 |
NG_008104.2:g.3559_3561delinsAGG , LRG_338:g.3559_3561delinsAGG | |
NG_008958.1:g.24831_24833delinsAGG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264156.3:c.1626+117_1626+119delinsAGG MANE Select | ENSP00000264156.2:n.1626+117_1626+119deli... | |
ENST00000264156.2:c.1626+117_1626+119delinsAGG | ENSP00000264156.2:n.1626+117_1626+119deli... | |
ENST00000492091.1:n.182-5048_182-5046delinsAGG | ||
NM_005915.5:c.1626+117_1626+119delinsAGG | NP_005906.2:n.1626+117_1626+119delinsAGG | |
NM_005915.6:c.1626+117_1626+119delinsAGG MANE Select | NP_005906.2:n.1626+117_1626+119delinsAGG |