HGVS | Genome Assembly |
---|---|
NC_000002.12:g.206122463del , CM000664.2:g.206122463del | GRCh38 |
NC_000002.11:g.206987187del , CM000664.1:g.206987187del | GRCh37 |
NC_000002.10:g.206695432del | NCBI36 |
NG_009248.1:g.42001del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000233190.11:c.*1722del MANE Select | ENSP00000233190.5:n.*1722del | |
ENST00000233190.10:c.*1722del | ENSP00000233190.5:n.*1722del | |
NM_001199981.2:c.*1722del | NP_001186910.1:n.*1722del | |
NM_001199982.2:c.*1722del | NP_001186911.1:n.*1722del | |
NM_001199983.2:c.*1722del | NP_001186912.1:n.*1722del | |
NM_005006.7:c.*1722del MANE Select | NP_004997.4:n.*1722del | |
NM_001199984.2:c.*1722del | NP_001186913.1:n.*1722del |