HGVS | Genome Assembly |
---|---|
NC_000012.12:g.91107175_91107176del , CM000674.2:g.91107175_91107176del | GRCh38 |
NC_000012.11:g.91500952_91500953del , CM000674.1:g.91500952_91500953del | GRCh37 |
NC_000012.10:g.90025083_90025084del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266718.5:c.862+942_862+943del MANE Select | ENSP00000266718.4:n.862+942_862+943del | |
ENST00000266718.4:c.862+942_862+943del | ENSP00000266718.4:n.862+942_862+943del | |
ENST00000546642.1:n.612+942_612+943del | ||
ENST00000548071.1:n.255+942_255+943del | ||
NM_002345.3:c.862+942_862+943del | NP_002336.1:n.862+942_862+943del | |
NM_002345.4:c.862+942_862+943del MANE Select | NP_002336.1:n.862+942_862+943del |