HGVS | Genome Assembly |
---|---|
NC_000022.11:g.39244746_39244759dup , CM000684.2:g.39244746_39244759dup | GRCh38 |
NC_000022.10:g.39640751_39640764dup , CM000684.1:g.39640751_39640764dup | GRCh37 |
NC_000022.9:g.37970697_37970710dup | NCBI36 |
NG_012111.1:g.5207_5220dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000331163.11:c.-783_-770dup MANE Select | ENSP00000330382.6:n.-783_-770dup | |
NM_002608.2:c.-783_-770dup | NP_002599.1:n.-783_-770dup | |
NM_002608.3:c.-783_-770dup | NP_002599.1:n.-783_-770dup | |
NM_002608.4:c.-783_-770dup MANE Select | NP_002599.1:n.-783_-770dup |