HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94842767_94842768delinsAC , CM000672.2:g.94842767_94842768delinsAC | GRCh38 |
NC_000010.10:g.96602524_96602525delinsAC , CM000672.1:g.96602524_96602525delinsAC | GRCh37 |
NC_000010.9:g.96592514_96592515delinsAC | NCBI36 |
NG_008384.2:g.85062_85063delinsAC | |
NG_008384.3:g.85087_85088delinsAC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000371321.9:c.962-70_962-69delinsAC MANE Select | ENSP00000360372.3:n.962-70_962-69delinsAC... | |
ENST00000645461.1:n.1873-70_1873-69delinsAC | ||
ENST00000371321.7:c.962-70_962-69delinsAC | ENSP00000360372.3:n.962-70_962-69delinsAC... | |
ENST00000464755.1:c.1725-70_1725-69delinsAC | ENSP00000483243.1:n.1725-70_1725-69delins... | |
NM_000769.2:c.962-70_962-69delinsAC | NP_000760.1:n.962-70_962-69delinsAC | |
NM_000769.4:c.962-70_962-69delinsAC MANE Select | NP_000760.1:n.962-70_962-69delinsAC |