Canonical Allele Identifier: CA12510037
Gene: KCTD7 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10263935

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.66631041G>A , CM000669.2:g.66631041G>A GRCh38
NC_000007.13:g.66096028G>A , CM000669.1:g.66096028G>A GRCh37
NC_000007.12:g.65733463G>A NCBI36
NG_028110.1:g.7161G>A
NG_028110.2:g.7161G>A

Transcript Alleles

HGVS Amino-acid change
NM_001167961.2:c.144+1833G>A VV NP_001161433.1:p.=
NM_153033.4:c.144+1833G>A VV NP_694578.1:p.=
ENST00000275532.7:c.144+1833G>A ENSP00000275532.3:p.=
ENST00000443322.1:c.144+1833G>A ENSP00000411624.1:p.=
ENST00000449064.5:c.144+1833G>A ENSP00000388463.1:p.=
ENST00000503687.1:c.144+1833G>A ENSP00000421074.1:p.=