Canonical Allele Identifier: CA9696190
Gene: ZNF805 HGNC NCBI

Linked Data

dbSNP Id: rs2014572

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.57248650G>A , CM000681.2:g.57248650G>A GRCh38
NC_000019.9:g.57760018G>A , CM000681.1:g.57760018G>A GRCh37
NC_000019.8:g.62451830G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000414468.3:c.203G>A MANE Select ENSP00000412999.1:p.Gly68Glu
ENST00000354309.4:c.-197G>A ENSP00000365414.2:n.-197G>A
ENST00000414468.2:c.203G>A ENSP00000412999.1:p.Gly68Glu
NM_001023563.3:c.203G>A NP_001018857.2:p.Gly68Glu
NM_001145078.1:c.-197G>A NP_001138550.1:n.-197G>A
NM_001023563.4:c.203G>A MANE Select NP_001018857.2:p.Gly68Glu
NM_001145078.2:c.-197G>A NP_001138550.1:n.-197G>A