HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41584034_41584039delinsTCTCTC , CM000679.2:g.41584034_41584039delinsTCTCTC | GRCh38 |
NC_000017.10:g.39740286_39740291delinsTCTCTC , CM000679.1:g.39740286_39740291delinsTCTCTC | GRCh37 |
NC_000017.9:g.36993812_36993817delinsTCTCTC | NCBI36 |
NG_008624.1:g.7857_7862delinsGAGAGA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000167586.7:c.766-118_766-113delinsGAGAGA MANE Select | ENSP00000167586.6:n.766-118_766-113delinsGAGAGA | |
ENST00000167586.6:c.766-118_766-113delinsGAGAGA | ENSP00000167586.6:n.766-118_766-113delinsGAGAGA | |
ENST00000476662.1:n.216-118_216-113delinsGAGAGA | ||
NM_000526.4:c.766-118_766-113delinsGAGAGA | NP_000517.2:n.766-118_766-113delinsGAGAGA | |
NM_000526.5:c.766-118_766-113delinsGAGAGA MANE Select | NP_000517.3:n.766-118_766-113delinsGAGAGA |