HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32202899_32202901del , CM000668.2:g.32202899_32202901del | GRCh38 |
NC_000006.11:g.32170676_32170678del , CM000668.1:g.32170676_32170678del | GRCh37 |
NC_000006.10:g.32278654_32278656del | NCBI36 |
NG_028190.1:g.26170_26172del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375023.3:c.3232-299_3232-297del MANE Select | ENSP00000364163.3:n.3232-299_3232-297del | |
ENST00000474612.1:n.1019_1021del | ||
NM_004557.3:c.3232-299_3232-297del | NP_004548.3:n.3232-299_3232-297del | |
NR_134949.1:n.3472+872_3472+874del | ||
NR_134950.1:n.3370+872_3370+874del | ||
NM_004557.4:c.3232-299_3232-297del MANE Select | NP_004548.3:n.3232-299_3232-297del | |
NR_134949.2:n.3472+872_3472+874del | ||
NR_134950.2:n.3370+872_3370+874del |