HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23433849_23433858del , CM000676.2:g.23433849_23433858del | GRCh38 |
NC_000014.8:g.23903058_23903067del , CM000676.1:g.23903058_23903067del | GRCh37 |
NC_000014.7:g.22972898_22972907del | NCBI36 |
NG_007884.1:g.6808_6817del , LRG_384:g.6808_6817del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.-8-114_-8-105del MANE Select | ENSP00000347507.3:n.-8-114_-8-105del | |
ENST00000355349.3:c.-8-114_-8-105del | ENSP00000347507.3:n.-8-114_-8-105del | |
NM_000257.3:c.-8-114_-8-105del | NP_000248.2:n.-8-114_-8-105del | |
XR_245686.3:n.99-114_99-105del | ||
XM_017021340.1:c.-8-114_-8-105del | XP_016876829.1:n.-8-114_-8-105del | |
NM_000257.4:c.-8-114_-8-105del MANE Select | NP_000248.2:n.-8-114_-8-105del |