HGVS | Genome Assembly |
---|---|
NC_000015.10:g.48481840dup , CM000677.2:g.48481840dup | GRCh38 |
NC_000015.9:g.48774037dup , CM000677.1:g.48774037dup | GRCh37 |
NC_000015.8:g.46561329dup | NCBI36 |
NG_008805.2:g.168952dup , LRG_778:g.168952dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000559133.6:c.3839-57dup | ENSP00000453958.2:n.3839-57dup | |
ENST00000674301.2:c.3839-57dup | ENSP00000501333.2:n.3839-57dup | |
ENST00000684448.1:n.2513-57dup | ||
ENST00000316623.10:c.3839-57dup MANE Select | ENSP00000325527.5:n.3839-57dup | |
ENST00000316623.9:c.3839-57dup | ENSP00000325527.5:n.3839-57dup | |
ENST00000537463.6:c.637-7187dup | ENSP00000440294.2:n.637-7187dup | |
NM_000138.4:c.3839-57dup , LRG_778t1:c.3839-57dup | NP_000129.3:n.3839-57dup | |
NM_000138.5:c.3839-57dup MANE Select | NP_000129.3:n.3839-57dup |