HGVS | Genome Assembly |
---|---|
NC_000001.11:g.215889074del , CM000663.2:g.215889074del | GRCh38 |
NC_000001.10:g.216062416del , CM000663.1:g.216062416del | GRCh37 |
NC_000001.9:g.214129039del | NCBI36 |
NG_009497.1:g.539324del | |
NG_009497.2:g.539376del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307340.8:c.7595-19del MANE Select | ENSP00000305941.3:n.7595-19del | |
ENST00000674083.1:c.7595-19del | ENSP00000501296.1:n.7595-19del | |
ENST00000307340.7:c.7595-19del | ENSP00000305941.3:n.7595-19del | |
NM_206933.2:c.7595-19del | NP_996816.2:n.7595-19del | |
NM_206933.3:c.7595-19del | NP_996816.2:n.7595-19del | |
NM_206933.4:c.7595-19del MANE Select | NP_996816.3:n.7595-19del |