HGVS | Genome Assembly |
---|---|
NC_000002.12:g.240877978del , CM000664.2:g.240877978del | GRCh38 |
NC_000002.11:g.241817395del , CM000664.1:g.241817395del | GRCh37 |
NC_000002.10:g.241466068del | NCBI36 |
NG_008005.1:g.14234del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307503.4:c.943-44del MANE Select | ENSP00000302620.3:n.943-44del | |
ENST00000307503.3:c.943-44del | ENSP00000302620.3:n.943-44del | |
ENST00000470255.1:n.721-44del | ||
NM_000030.2:c.943-44del | NP_000021.1:n.943-44del | |
NM_000030.3:c.943-44del MANE Select | NP_000021.1:n.943-44del |