HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23431027del , CM000676.2:g.23431027del | GRCh38 |
NC_000014.8:g.23900236del , CM000676.1:g.23900236del | GRCh37 |
NC_000014.7:g.22970076del | NCBI36 |
NG_007884.1:g.9635del , LRG_384:g.9635del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.797-28del MANE Select | ENSP00000347507.3:n.797-28del | |
ENST00000355349.3:c.797-28del | ENSP00000347507.3:n.797-28del | |
NM_000257.3:c.797-28del | NP_000248.2:n.797-28del | |
XR_245686.3:n.903-28del | ||
XM_017021340.1:c.797-28del | XP_016876829.1:n.797-28del | |
NM_000257.4:c.797-28del MANE Select | NP_000248.2:n.797-28del |