HGVS | Genome Assembly |
---|---|
NC_000002.12:g.73640860del , CM000664.2:g.73640860del | GRCh38 |
NC_000002.11:g.73867987del , CM000664.1:g.73867987del | GRCh37 |
NC_000002.10:g.73721495del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000272425.4:c.*85del MANE Select | ENSP00000272425.3:n.*85del | |
ENST00000272425.3:c.*85del | ENSP00000272425.3:n.*85del | |
NM_003960.3:c.*85del | NP_003951.3:n.*85del | |
NM_003960.4:c.*85del MANE Select | NP_003951.3:n.*85del |