HGVS | Genome Assembly |
---|---|
NC_000019.10:g.39247894_39247913dup , CM000681.2:g.39247894_39247913dup | GRCh38 |
NC_000019.9:g.39738534_39738553dup , CM000681.1:g.39738534_39738553dup | GRCh37 |
NC_000019.8:g.44430374_44430393dup | NCBI36 |
NG_042193.1:g.2061_2080dup | |
NG_055295.1:g.5946_5965dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000606380.2:c.223+13_223+32dup | ENSP00000476098.1:n.223+13_223+32dup | |
ENST00000610963.1:c.222+13_222+32dup | ENSP00000481371.1:n.222+13_222+32dup | |
ENST00000616270.4:c.223+13_223+32dup | ENSP00000480679.1:n.223+13_223+32dup | |
ENST00000634680.1:c.152-448_152-429dup | ENSP00000489240.1:n.152-448_152-429dup | |
ENST00000634967.1:c.223+13_223+32dup | ENSP00000489559.1:n.223+13_223+32dup | |
NR_074079.1:n.500+13_500+32dup |