HGVS | Genome Assembly |
---|---|
NC_000008.11:g.6877909_6877910insT , CM000670.2:g.6877909_6877910insT | GRCh38 |
NC_000008.10:g.6735431_6735432insT , CM000670.1:g.6735431_6735432insT | GRCh37 |
NC_000008.9:g.6722841_6722842insT | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000297439.4:c.-53_-52insA MANE Select | ENSP00000297439.3:n.-53_-52insA | |
ENST00000297439.3:c.-53_-52insA | ENSP00000297439.3:n.-53_-52insA | |
NM_005218.3:c.-53_-52insA | NP_005209.1:n.-53_-52insA | |
NM_005218.4:c.-53_-52insA MANE Select | NP_005209.1:n.-53_-52insA |