HGVS | Genome Assembly |
---|---|
NC_000002.12:g.135856504_135856505delinsAC , CM000664.2:g.135856504_135856505delinsAC | GRCh38 |
NC_000002.11:g.136614074_136614075delinsAC , CM000664.1:g.136614074_136614075delinsAC | GRCh37 |
NC_000002.10:g.136330544_136330545delinsAC | NCBI36 |
NG_008104.2:g.3665_3666delinsGT , LRG_338:g.3665_3666delinsGT | |
NG_008958.1:g.24937_24938delinsGT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264156.3:c.1626+223_1626+224delinsGT MANE Select | ENSP00000264156.2:n.1626+223_1626+224delinsGT | |
ENST00000264156.2:c.1626+223_1626+224delinsGT | ENSP00000264156.2:n.1626+223_1626+224delinsGT | |
ENST00000492091.1:n.182-4942_182-4941delinsGT | ||
NM_005915.5:c.1626+223_1626+224delinsGT | NP_005906.2:n.1626+223_1626+224delinsGT | |
NM_005915.6:c.1626+223_1626+224delinsGT MANE Select | NP_005906.2:n.1626+223_1626+224delinsGT |