Canonical Allele Identifier: CA472908972
Gene: CAVIN3 HGNC NCBI

Linked Data

dbSNP Id: rs1846779163
gnomAD v3: 11-6319475-C-T
gnomAD v4: 11-6319475-C-T
COSMIC: COSM4940353
MyVariant Identifiers: chr11:g.6340705C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6319475C>T , CM000673.2:g.6319475C>T GRCh38
NC_000011.9:g.6340705C>T , CM000673.1:g.6340705C>T GRCh37
NC_000011.8:g.6297281C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303927.4:c.474G>A MANE Select ENSP00000307292.3:p.Leu158=
ENST00000303927.3:c.474G>A ENSP00000307292.3:p.Leu158=
ENST00000524852.1:n.260G>A
ENST00000530979.1:c.570G>A ENSP00000432047.1:p.Leu190=
ENST00000532354.1:n.496G>A
NM_145040.2:c.474G>A NP_659477.2:p.Leu158=
XR_930997.1:n.720+1255C>T
XR_001748106.1:n.86C>T
XR_242848.4:n.335C>T
NM_145040.3:c.474G>A MANE Select NP_659477.2:p.Leu158=
Search 100 bp 5'
Search 100 bp 3'