HGVS | Genome Assembly |
---|---|
NC_000002.12:g.26135213_26135216dup , CM000664.2:g.26135213_26135216dup | GRCh38 |
NC_000002.11:g.26358082_26358085dup , CM000664.1:g.26358082_26358085dup | GRCh37 |
NC_000002.10:g.26211586_26211589dup | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264710.5:c.*192_*195dup MANE Select | ENSP00000264710.4:n.*192_*195dup | |
ENST00000264710.4:c.*192_*195dup | ENSP00000264710.4:n.*192_*195dup | |
ENST00000495146.5:n.1158_1161dup | ||
NM_016131.4:c.*192_*195dup | NP_057215.3:n.*192_*195dup | |
XM_024452565.1:c.*192_*195dup | XP_024308333.1:n.*192_*195dup | |
NM_016131.5:c.*192_*195dup MANE Select | NP_057215.3:n.*192_*195dup |