Canonical Allele Identifier: CA1493209

Gene: ZNF670 ZNF670-ZNF695

Linked Data

• ClinVar Variation Id: 2465277
• ClinVar RCV Id: RCV004258371
• dbSNP Id: rs201647737
• ExAC: 1:247201580 C / T
• gnomAD v2: 1-247201580-C-T
• gnomAD v3: 1-247038278-C-T
• gnomAD v4: 1-247038278-C-T
• MyVariant Identifiers: chr1:g.247201580C>T (hg19) ; chr1:g.247201580_247201582delinsTAT (hg19) ; chr1:g.247038278C>T (hg38) ; chr1:g.247038278_247038280delinsTAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.247038278C>T , CM000663.2:g.247038278C>T	GRCh38
NC_000001.10:g.247201580C>T , CM000663.1:g.247201580C>T	GRCh37
NC_000001.9:g.245268203C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366503.3:c.341G>A (ZNF670) MANE Select	ENSP00000355459.2:p.Cys114Tyr
ENST00000366503.2:c.341G>A (ZNF670)	ENSP00000355459.2:p.Cys114Tyr
ENST00000465049.6:c.4-38204G>A (ZNF670-ZNF695)	ENSP00000428213.1:n.4-38204G>A
ENST00000474541.1:c.4-38204G>A (ZNF670-ZNF695)	ENSP00000428036.1:n.4-38204G>A
NM_001204220.1:c.338G>A (ZNF670)	NP_001191149.1:p.Cys113Tyr
NM_033213.4:c.341G>A (ZNF670)	NP_149990.1:p.Cys114Tyr
NR_037894.1:n.221-38204G>A (ZNF670-ZNF695)
NM_033213.5:c.341G>A (ZNF670) MANE Select	NP_149990.1:p.Cys114Tyr
NM_001204220.2:c.338G>A (ZNF670)	NP_001191149.1:p.Cys113Tyr
NR_037894.2:n.219-38204G>A (ZNF670-ZNF695)