HGVS | Genome Assembly |
---|---|
NC_000002.12:g.26135233_26135234del , CM000664.2:g.26135233_26135234del | GRCh38 |
NC_000002.11:g.26358102_26358103del , CM000664.1:g.26358102_26358103del | GRCh37 |
NC_000002.10:g.26211606_26211607del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264710.5:c.*212_*213del MANE Select | ENSP00000264710.4:n.*212_*213del | |
ENST00000264710.4:c.*212_*213del | ENSP00000264710.4:n.*212_*213del | |
ENST00000495146.5:n.1178_1179del | ||
NM_016131.4:c.*212_*213del | NP_057215.3:n.*212_*213del | |
XM_024452565.1:c.*212_*213del | XP_024308333.1:n.*212_*213del | |
NM_016131.5:c.*212_*213del MANE Select | NP_057215.3:n.*212_*213del |