HGVS | Genome Assembly |
---|---|
NC_000013.11:g.48045584_48045585dup , CM000675.2:g.48045584_48045585dup | GRCh38 |
NC_000013.10:g.48619720_48619721dup , CM000675.1:g.48619720_48619721dup | GRCh37 |
NC_000013.9:g.47517721_47517722dup | NCBI36 |
NG_047021.1:g.13018_13019dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000258662.3:c.356-76_356-75dup MANE Select | ENSP00000258662.1:n.356-76_356-75dup | |
ENST00000258662.2:c.356-76_356-75dup | ENSP00000258662.1:n.356-76_356-75dup | |
NM_018283.2:c.356-76_356-75dup | NP_060753.1:n.356-76_356-75dup | |
NM_018283.3:c.356-76_356-75dup | NP_060753.1:n.356-76_356-75dup | |
NR_136687.1:n.536-76_536-75dup | ||
NR_136688.1:n.536-76_536-75dup | ||
NM_018283.4:c.356-76_356-75dup MANE Select | NP_060753.1:n.356-76_356-75dup | |
NR_136687.2:n.377-76_377-75dup | ||
NR_136688.2:n.377-76_377-75dup |