HGVS | Genome Assembly |
---|---|
NC_000002.12:g.189001320del , CM000664.2:g.189001320del | GRCh38 |
NC_000002.11:g.189866046del , CM000664.1:g.189866046del | GRCh37 |
NC_000002.10:g.189574291del | NCBI36 |
NG_007404.1:g.31948del , LRG_3:g.31948del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000450867.2:c.2185-77del | ENSP00000415346.2:n.2185-77del | |
ENST00000304636.9:c.2284-77del MANE Select | ENSP00000304408.4:n.2284-77del | |
ENST00000304636.7:c.2284-77del | ENSP00000304408.3:n.2284-77del | |
ENST00000317840.9:c.2284-77del | ENSP00000315243.6:n.2284-77del | |
NM_000090.3:c.2284-77del , LRG_3t1:c.2284-77del | NP_000081.1:n.2284-77del | |
NM_000090.4:c.2284-77del MANE Select | NP_000081.2:n.2284-77del |