HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94842776_94842783dup , CM000672.2:g.94842776_94842783dup | GRCh38 |
NC_000010.10:g.96602533_96602540dup , CM000672.1:g.96602533_96602540dup | GRCh37 |
NC_000010.9:g.96592523_96592530dup | NCBI36 |
NG_008384.2:g.85071_85078dup | |
NG_008384.3:g.85096_85103dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000371321.9:c.962-61_962-54dup MANE Select | ENSP00000360372.3:n.962-61_962-54dup | |
ENST00000645461.1:n.1873-61_1873-54dup | ||
ENST00000371321.7:c.962-61_962-54dup | ENSP00000360372.3:n.962-61_962-54dup | |
ENST00000464755.1:c.1725-61_1725-54dup | ENSP00000483243.1:n.1725-61_1725-54dup | |
NM_000769.2:c.962-61_962-54dup | NP_000760.1:n.962-61_962-54dup | |
NM_000769.4:c.962-61_962-54dup MANE Select | NP_000760.1:n.962-61_962-54dup |