Canonical Allele Identifier: CA472720328
Gene: CAVIN3 HGNC NCBI

Linked Data

gnomAD v4: 11-6319193-T-C
MyVariant Identifiers: chr11:g.6340423T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6319193T>C , CM000673.2:g.6319193T>C GRCh38
NC_000011.9:g.6340423T>C , CM000673.1:g.6340423T>C GRCh37
NC_000011.8:g.6296999T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000303927.4:c.756A>G MANE Select ENSP00000307292.3:p.Glu252=
ENST00000303927.3:c.756A>G ENSP00000307292.3:p.Glu252=
ENST00000524852.1:n.542A>G
ENST00000530979.1:c.852A>G ENSP00000432047.1:p.Glu284=
ENST00000532354.1:n.778A>G
NM_145040.2:c.756A>G NP_659477.2:p.Glu252=
XR_930997.1:n.720+973T>C
XR_242848.4:n.53T>C
NM_145040.3:c.756A>G MANE Select NP_659477.2:p.Glu252=