HGVS | Genome Assembly |
---|---|
NC_000015.10:g.74754805_74754806delinsAC , CM000677.2:g.74754805_74754806delinsAC | GRCh38 |
NC_000015.9:g.75047146_75047147delinsAC , CM000677.1:g.75047146_75047147delinsAC | GRCh37 |
NC_000015.8:g.72834199_72834200delinsAC | NCBI36 |
NG_008431.1:g.37264_37265delinsAC | |
NG_008431.2:g.37264_37265delinsAC | |
NG_061543.1:g.10961_10962delinsAC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000343932.5:c.1268_1269delinsAC MANE Select | ENSP00000342007.4:p.Asp423= | |
ENST00000343932.4:c.1268_1269delinsAC | ENSP00000342007.4:p.Asp423= | |
NM_000761.4:c.1268_1269delinsAC | NP_000752.2:p.Asp423= | |
NM_000761.5:c.1268_1269delinsAC MANE Select | NP_000752.2:p.Asp423= |