HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32202689_32202690del , CM000668.2:g.32202689_32202690del | GRCh38 |
NC_000006.11:g.32170466_32170467del , CM000668.1:g.32170466_32170467del | GRCh37 |
NC_000006.10:g.32278444_32278445del | NCBI36 |
NG_028190.1:g.26380_26381del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375023.3:c.3232-89_3232-88del MANE Select | ENSP00000364163.3:n.3232-89_3232-88del | |
ENST00000474612.1:n.1229_1230del | ||
NM_004557.3:c.3232-89_3232-88del | NP_004548.3:n.3232-89_3232-88del | |
NR_134949.1:n.3472+1082_3472+1083del | ||
NR_134950.1:n.3370+1082_3370+1083del | ||
NM_004557.4:c.3232-89_3232-88del MANE Select | NP_004548.3:n.3232-89_3232-88del | |
NR_134949.2:n.3472+1082_3472+1083del | ||
NR_134950.2:n.3370+1082_3370+1083del |