HGVS | Genome Assembly |
---|---|
NC_000023.11:g.78117302_78117303dup , CM000685.2:g.78117302_78117303dup | GRCh38 |
NC_000023.10:g.77372799_77372800dup , CM000685.1:g.77372799_77372800dup | GRCh37 |
NC_000023.9:g.77259455_77259456dup | NCBI36 |
NG_008862.1:g.18134_18135dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000373316.5:c.418-10_418-9dup MANE Select | ENSP00000362413.4:n.418-10_418-9dup | |
ENST00000644362.1:c.334-10_334-9dup | ENSP00000496140.1:n.334-10_334-9dup | |
ENST00000373316.4:c.418-10_418-9dup | ENSP00000362413.4:n.418-10_418-9dup | |
ENST00000491291.1:n.410-10_410-9dup | ||
NM_000291.3:c.418-10_418-9dup | NP_000282.1:n.418-10_418-9dup | |
NM_000291.4:c.418-10_418-9dup MANE Select | NP_000282.1:n.418-10_418-9dup |