HGVS | Genome Assembly |
---|---|
NC_000019.10:g.18785930_18785933dup , CM000681.2:g.18785930_18785933dup | GRCh38 |
NC_000019.9:g.18896740_18896743dup , CM000681.1:g.18896740_18896743dup | GRCh37 |
NC_000019.8:g.18757740_18757743dup | NCBI36 |
NG_007070.1:g.10372_10375dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000222271.7:c.1489+32_1489+35dup MANE Select | ENSP00000222271.2:n.1489+32_1489+35dup | |
ENST00000222271.6:c.1489+32_1489+35dup | ENSP00000222271.2:n.1489+32_1489+35dup | |
ENST00000425807.1:c.1330+32_1330+35dup | ENSP00000403792.1:n.1330+32_1330+35dup | |
ENST00000542601.6:c.1390+32_1390+35dup | ENSP00000439156.2:n.1390+32_1390+35dup | |
NM_000095.2:c.1489+32_1489+35dup | NP_000086.2:n.1489+32_1489+35dup | |
NM_000095.3:c.1489+32_1489+35dup MANE Select | NP_000086.2:n.1489+32_1489+35dup |