Canonical Allele Identifier: CA1950112471
Gene: CAVIN3 HGNC NCBI

Linked Data

dbSNP Id: rs1846763269
gnomAD v4: 11-6319094-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6319094G>C , CM000673.2:g.6319094G>C GRCh38
NC_000011.9:g.6340324G>C , CM000673.1:g.6340324G>C GRCh37
NC_000011.8:g.6296900G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000303927.4:c.*69C>G MANE Select ENSP00000307292.3:n.*69C>G
ENST00000303927.3:c.*69C>G ENSP00000307292.3:n.*69C>G
ENST00000532354.1:n.877C>G
NM_145040.2:c.*69C>G NP_659477.2:n.*69C>G
XR_930997.1:n.720+874G>C
NM_145040.3:c.*69C>G MANE Select NP_659477.2:n.*69C>G