HGVS | Genome Assembly |
---|---|
NC_000002.12:g.135856585_135856586insACC , CM000664.2:g.135856585_135856586insACC | GRCh38 |
NC_000002.11:g.136614155_136614156insACC , CM000664.1:g.136614155_136614156insACC | GRCh37 |
NC_000002.10:g.136330625_136330626insACC | NCBI36 |
NG_008104.2:g.3584_3585insGGT , LRG_338:g.3584_3585insGGT | |
NG_008958.1:g.24856_24857insGGT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264156.3:c.1626+142_1626+143insGGT MANE Select | ENSP00000264156.2:n.1626+142_1626+143insG... | |
ENST00000264156.2:c.1626+142_1626+143insGGT | ENSP00000264156.2:n.1626+142_1626+143insG... | |
ENST00000492091.1:n.182-5023_182-5022insGGT | ||
NM_005915.5:c.1626+142_1626+143insGGT | NP_005906.2:n.1626+142_1626+143insGGT | |
NM_005915.6:c.1626+142_1626+143insGGT MANE Select | NP_005906.2:n.1626+142_1626+143insGGT |