Canonical Allele Identifier: CA14705050
Gene: ZNF610 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2657940

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.52360583G>A , CM000681.2:g.52360583G>A GRCh38
NC_000019.9:g.52863836G>A , CM000681.1:g.52863836G>A GRCh37
NC_000019.8:g.57555648G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001161425.1:c.320-5115G>A VV NP_001154897.1:p.=
NM_001161426.1:c.320-5115G>A VV NP_001154898.1:p.=
NM_001161427.1:c.191-5115G>A VV NP_001154899.1:p.=
NM_173530.2:c.320-5115G>A VV NP_775801.2:p.=
XM_011526560.1:c.320-5115G>A XP_011524862.1:p.=
XM_011526561.1:c.320-5115G>A XP_011524863.1:p.=
XM_011526562.1:c.320-5115G>A XP_011524864.1:p.=
NM_001161425.2:c.320-5115G>A VV MANE Preferred NP_001154897.1:p.=
ENST00000321287.12:c.320-5115G>A ENSP00000324441.8:p.=
ENST00000327920.12:c.320-5115G>A ENSP00000327597.7:p.=
ENST00000403906.7:c.320-5115G>A ENSP00000383922.2:p.=
ENST00000601151.5:c.191-5115G>A ENSP00000471021.1:p.=
ENST00000613461.3:c.191-5115G>A ENSP00000477617.1:p.=
ENST00000616431.2:c.320-5115G>A ENSP00000485001.1:p.=