HGVS | Genome Assembly |
---|---|
NC_000013.11:g.48045951_48045952del , CM000675.2:g.48045951_48045952del | GRCh38 |
NC_000013.10:g.48620087_48620088del , CM000675.1:g.48620087_48620088del | GRCh37 |
NC_000013.9:g.47518088_47518089del | NCBI36 |
NG_047021.1:g.13385_13386del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000258662.3:c.*152_*153del MANE Select | ENSP00000258662.1:n.*152_*153del | |
ENST00000258662.2:c.*152_*153del | ENSP00000258662.1:n.*152_*153del | |
NM_018283.2:c.*152_*153del | NP_060753.1:n.*152_*153del | |
NM_018283.3:c.*152_*153del | NP_060753.1:n.*152_*153del | |
NR_136687.1:n.718+109_718+110del | ||
NR_136688.1:n.675+152_675+153del | ||
NM_018283.4:c.*152_*153del MANE Select | NP_060753.1:n.*152_*153del | |
NR_136687.2:n.559+109_559+110del | ||
NR_136688.2:n.516+152_516+153del |