HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41584099_41584100del , CM000679.2:g.41584099_41584100del | GRCh38 |
NC_000017.10:g.39740351_39740352del , CM000679.1:g.39740351_39740352del | GRCh37 |
NC_000017.9:g.36993877_36993878del | NCBI36 |
NG_008624.1:g.7796_7797del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000167586.7:c.765+157_765+158del MANE Select | ENSP00000167586.6:n.765+157_765+158del | |
ENST00000167586.6:c.765+157_765+158del | ENSP00000167586.6:n.765+157_765+158del | |
ENST00000476662.1:n.215+157_215+158del | ||
NM_000526.4:c.765+157_765+158del | NP_000517.2:n.765+157_765+158del | |
NM_000526.5:c.765+157_765+158del MANE Select | NP_000517.3:n.765+157_765+158del |