HGVS | Genome Assembly |
---|---|
NC_000022.11:g.37710390_37710391dup , CM000684.2:g.37710390_37710391dup | GRCh38 |
NC_000022.10:g.38106397_38106398dup , CM000684.1:g.38106397_38106398dup | GRCh37 |
NC_000022.9:g.36436343_36436344dup | NCBI36 |
NG_012857.1:g.18403_18404dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000644935.1:c.115-37_115-36dup MANE Select | ENSP00000496394.1:n.115-37_115-36dup | |
ENST00000344404.10:c.115-37_115-36dup | ENSP00000340312.6:n.115-37_115-36dup | |
ENST00000406386.7:c.115-37_115-36dup | ENSP00000384312.3:n.115-37_115-36dup | |
ENST00000455236.4:c.1072-37_1072-36dup | ENSP00000477208.1:n.1072-37_1072-36dup | |
ENST00000492485.5:n.251-37_251-36dup | ||
NM_001039141.2:c.115-37_115-36dup | NP_001034230.1:n.115-37_115-36dup | |
NM_001039141.3:c.115-37_115-36dup MANE Select | NP_001034230.1:n.115-37_115-36dup |