HGVS | Genome Assembly |
---|---|
NC_000012.12:g.6031661_6031662del , CM000674.2:g.6031661_6031662del | GRCh38 |
NC_000012.11:g.6140827_6140828del , CM000674.1:g.6140827_6140828del | GRCh37 |
NC_000012.10:g.6011088_6011089del | NCBI36 |
NG_009072.1:g.98009_98010del | |
NG_009072.2:g.98009_98010del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261405.10:c.2686-84_2686-83del MANE Select | ENSP00000261405.5:n.2686-84_2686-83del | |
ENST00000261405.9:c.2686-84_2686-83del | ENSP00000261405.5:n.2686-84_2686-83del | |
ENST00000538635.5:n.421-37728_421-37727del | ||
NM_000552.3:c.2686-84_2686-83del | NP_000543.2:n.2686-84_2686-83del | |
NM_000552.4:c.2686-84_2686-83del | NP_000543.2:n.2686-84_2686-83del | |
NM_000552.5:c.2686-84_2686-83del MANE Select | NP_000543.3:n.2686-84_2686-83del |