HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41584077_41584098dup , CM000679.2:g.41584077_41584098dup | GRCh38 |
NC_000017.10:g.39740329_39740350dup , CM000679.1:g.39740329_39740350dup | GRCh37 |
NC_000017.9:g.36993855_36993876dup | NCBI36 |
NG_008624.1:g.7805_7826dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000167586.7:c.765+166_766-149dup MANE Select | ENSP00000167586.6:n.765+166_766-149dup | |
ENST00000167586.6:c.765+166_766-149dup | ENSP00000167586.6:n.765+166_766-149dup | |
ENST00000476662.1:n.215+166_216-149dup | ||
NM_000526.4:c.765+166_766-149dup | NP_000517.2:n.765+166_766-149dup | |
NM_000526.5:c.765+166_766-149dup MANE Select | NP_000517.3:n.765+166_766-149dup |