Canonical Allele Identifier: CA10610069
Gene: GJB3 HGNC NCBI
SMIM12 HGNC NCBI

Linked Data

ClinVar Variation Id: 297182
ClinVar RCV Id: RCV000363945
dbSNP Id: rs1057515476
MyVariant Identifiers: chr1:g.35247022G>A (hg19) chr1:g.34781421G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34781421G>A , CM000663.2:g.34781421G>A GRCh38
NC_000001.10:g.35247022G>A , CM000663.1:g.35247022G>A GRCh37
NC_000001.9:g.35019609G>A NCBI36
NG_008309.1:g.5233G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000373366.3:c.-383G>A (GJB3) MANE Select ENSP00000362464.2:n.-383G>A
ENST00000373366.2:c.-383G>A (GJB3) ENSP00000362464.2:n.-383G>A
ENST00000426886.1:c.208-63012C>T (SMIM12) ENSP00000429902.1:n.208-63012C>T
NM_024009.2:c.-383G>A (GJB3) NP_076872.1:n.-383G>A
XR_947179.1:n.1001+16950C>T
XR_001737967.1:n.1023+16950C>T
NM_024009.3:c.-383G>A (GJB3) MANE Select NP_076872.1:n.-383G>A
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