HGVS | Genome Assembly |
---|---|
NC_000001.11:g.215867254_215867257del , CM000663.2:g.215867254_215867257del | GRCh38 |
NC_000001.10:g.216040596_216040599del , CM000663.1:g.216040596_216040599del | GRCh37 |
NC_000001.9:g.214107219_214107222del | NCBI36 |
NG_009497.1:g.561141_561144del | |
NG_009497.2:g.561193_561196del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307340.8:c.8682-86_8682-83del MANE Select | ENSP00000305941.3:n.8682-86_8682-83del | |
ENST00000674083.1:c.8682-86_8682-83del | ENSP00000501296.1:n.8682-86_8682-83del | |
ENST00000307340.7:c.8682-86_8682-83del | ENSP00000305941.3:n.8682-86_8682-83del | |
NM_206933.2:c.8682-86_8682-83del | NP_996816.2:n.8682-86_8682-83del | |
NM_206933.3:c.8682-86_8682-83del | NP_996816.2:n.8682-86_8682-83del | |
NM_206933.4:c.8682-86_8682-83del MANE Select | NP_996816.3:n.8682-86_8682-83del |