Canonical Allele Identifier: CA379352281
Gene: CAVIN3 HGNC NCBI

Linked Data

dbSNP Id: rs1427872531
gnomAD v2: 11-6340634-C-A
gnomAD v4: 11-6319404-C-A
MyVariant Identifiers: chr11:g.6340634C>A (hg19) chr11:g.6319404C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6319404C>A , CM000673.2:g.6319404C>A GRCh38
NC_000011.9:g.6340634C>A , CM000673.1:g.6340634C>A GRCh37
NC_000011.8:g.6297210C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303927.4:c.545G>T MANE Select ENSP00000307292.3:p.Gly182Val
ENST00000303927.3:c.545G>T ENSP00000307292.3:p.Gly182Val
ENST00000524852.1:n.331G>T
ENST00000530979.1:c.641G>T ENSP00000432047.1:p.Gly214Val
ENST00000532354.1:n.567G>T
NM_145040.2:c.545G>T NP_659477.2:p.Gly182Val
XR_930997.1:n.720+1184C>A
XR_001748106.1:n.15C>A
XR_242848.4:n.264C>A
NM_145040.3:c.545G>T MANE Select NP_659477.2:p.Gly182Val
Search 100 bp 5'
Search 100 bp 3'