Canonical Allele Identifier: CA5852181
Gene: CAVIN3 HGNC NCBI

Linked Data

dbSNP Id: rs762061933
gnomAD v2: 11-6340406-T-C
gnomAD v3: 11-6319176-T-C
gnomAD v4: 11-6319176-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6319176T>C , CM000673.2:g.6319176T>C GRCh38
NC_000011.9:g.6340406T>C , CM000673.1:g.6340406T>C GRCh37
NC_000011.8:g.6296982T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303927.4:c.773A>G MANE Select ENSP00000307292.3:p.Glu258Gly
ENST00000303927.3:c.773A>G ENSP00000307292.3:p.Glu258Gly
ENST00000524852.1:n.559A>G
ENST00000530979.1:c.869A>G ENSP00000432047.1:p.Glu290Gly
ENST00000532354.1:n.795A>G
NM_145040.2:c.773A>G NP_659477.2:p.Glu258Gly
XR_930997.1:n.720+956T>C
XR_242848.4:n.36T>C
NM_145040.3:c.773A>G MANE Select NP_659477.2:p.Glu258Gly