Canonical Allele Identifier: CA1950112428
Gene: CAVIN3 HGNC NCBI

Linked Data

dbSNP Id: rs1846761085
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6319024G>C , CM000673.2:g.6319024G>C GRCh38
NC_000011.9:g.6340254G>C , CM000673.1:g.6340254G>C GRCh37
NC_000011.8:g.6296830G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303927.4:c.*139C>G MANE Select ENSP00000307292.3:n.*139C>G
ENST00000303927.3:c.*139C>G ENSP00000307292.3:n.*139C>G
ENST00000532354.1:n.947C>G
NM_145040.2:c.*139C>G NP_659477.2:n.*139C>G
XR_930997.1:n.720+804G>C
NM_145040.3:c.*139C>G MANE Select NP_659477.2:n.*139C>G
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