HGVS | Genome Assembly |
---|---|
NC_000014.9:g.28768340_28768341delinsAC , CM000676.2:g.28768340_28768341delinsAC | GRCh38 |
NC_000014.8:g.29237546_29237547delinsAC , CM000676.1:g.29237546_29237547delinsAC | GRCh37 |
NC_000014.7:g.28307297_28307298delinsAC | NCBI36 |
NG_009367.1:g.6260_6261delinsAC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706482.1:c.1061_1062delinsAC | ENSP00000516406.1:p.His354= | |
ENST00000313071.7:c.1061_1062delinsAC MANE Select | ENSP00000339004.3:p.His354= | |
ENST00000313071.6:c.1061_1062delinsAC | ENSP00000339004.3:p.His354= | |
NM_005249.4:c.1061_1062delinsAC | NP_005240.3:p.His354= | |
NM_005249.5:c.1061_1062delinsAC MANE Select | NP_005240.3:p.His354= |