Canonical Allele Identifier: CA143806
Gene: DUSP6 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 50854
ClinVar RCV Id: RCV000043594
dbSNP Id: rs143946794

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.89350860T>C , CM000674.2:g.89350860T>C GRCh38
NC_000012.11:g.89744637T>C , CM000674.1:g.89744637T>C GRCh37
NC_000012.10:g.88268768T>C NCBI36
NG_033915.1:g.7000A>G

Transcript Alleles

HGVS Amino-acid change
NM_001946.3:c.566A>G VV NP_001937.2:p.Asn189Ser
NM_022652.3:c.400+780A>G VV NP_073143.2:p.=
ENST00000279488.7:c.566A>G ENSP00000279488.6:p.Asn189Ser
ENST00000308385.6:c.400+780A>G ENSP00000307835.6:p.=
ENST00000547140.1:n.252A>G
ENST00000547291.1:c.191A>G ENSP00000449838.1:p.Asn64Ser