Canonical Allele Identifier: CA199714

Gene: FZD6

Linked Data

• ClinVar Variation Id: 190461
• ClinVar RCV Id: RCV000170581 ; RCV001329712
• dbSNP Id: rs786205672
• MyVariant Identifiers: chr8:g.104337203A>G (hg19) ; chr8:g.103324975A>G (hg38)
• PubMed: PMID:26036949

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.103324975A>G , CM000670.2:g.103324975A>G	GRCh38
NC_000008.10:g.104337203A>G , CM000670.1:g.104337203A>G	GRCh37
NC_000008.9:g.104406379A>G	NCBI36
NG_028909.1:g.31543A>G
NG_028909.2:g.28982A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358755.5:c.869A>G MANE Select	ENSP00000351605.4:p.Tyr290Cys
ENST00000358755.4:c.869A>G	ENSP00000351605.4:p.Tyr290Cys
ENST00000519011.5:c.178-79A>G	ENSP00000427733.1:n.178-79A>G
ENST00000521195.1:c.*804A>G	ENSP00000428188.1:n.*804A>G
ENST00000522484.5:c.869A>G	ENSP00000428301.1:p.Tyr290Cys
ENST00000522566.5:c.869A>G	ENSP00000429055.1:p.Tyr290Cys
ENST00000523739.5:c.773A>G	ENSP00000429528.1:p.Tyr258Cys
ENST00000523933.5:c.279-60A>G	ENSP00000428257.1:n.279-60A>G
NM_001164615.1:c.869A>G	NP_001158087.1:p.Tyr290Cys
NM_001164616.1:c.773A>G	NP_001158088.1:p.Tyr258Cys
NM_003506.3:c.869A>G	NP_003497.2:p.Tyr290Cys
XR_428385.2:n.1119A>G
NM_001317796.1:c.33-79A>G	NP_001304725.1:n.33-79A>G
NR_133921.1:n.1186A>G
NM_003506.4:c.869A>G MANE Select	NP_003497.2:p.Tyr290Cys
NM_001164615.2:c.869A>G	NP_001158087.1:p.Tyr290Cys
NM_001164616.2:c.773A>G	NP_001158088.1:p.Tyr258Cys
NM_001317796.2:c.33-79A>G	NP_001304725.1:n.33-79A>G
NR_133921.2:n.1186A>G