HGVS | Genome Assembly |
---|---|
NC_000001.11:g.204165319_204165321dup , CM000663.2:g.204165319_204165321dup | GRCh38 |
NC_000001.10:g.204134447_204134449dup , CM000663.1:g.204134447_204134449dup | GRCh37 |
NC_000001.9:g.202401070_202401072dup | NCBI36 |
NG_012122.1:g.6019_6021dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000272190.9:c.98+877_98+879dup MANE Select | ENSP00000272190.8:n.98+877_98+879dup | |
ENST00000638118.1:c.-16-3156_-16-3154dup | ENSP00000490307.1:n.-16-3156_-16-3154dup | |
ENST00000272190.8:c.98+877_98+879dup | ENSP00000272190.8:n.98+877_98+879dup | |
NM_000537.3:c.98+877_98+879dup | NP_000528.1:n.98+877_98+879dup | |
NM_000537.4:c.98+877_98+879dup MANE Select | NP_000528.1:n.98+877_98+879dup |