HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23431880_23431881del , CM000676.2:g.23431880_23431881del | GRCh38 |
NC_000014.8:g.23901089_23901090del , CM000676.1:g.23901089_23901090del | GRCh37 |
NC_000014.7:g.22970929_22970930del | NCBI36 |
NG_007884.1:g.8781_8782del , LRG_384:g.8781_8782del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.531-12_531-11del MANE Select | ENSP00000347507.3:n.531-12_531-11del | |
ENST00000355349.3:c.531-12_531-11del | ENSP00000347507.3:n.531-12_531-11del | |
NM_000257.3:c.531-12_531-11del | NP_000248.2:n.531-12_531-11del | |
XR_245686.3:n.637-12_637-11del | ||
XM_017021340.1:c.531-12_531-11del | XP_016876829.1:n.531-12_531-11del | |
NM_000257.4:c.531-12_531-11del MANE Select | NP_000248.2:n.531-12_531-11del |