Canonical Allele Identifier: CA257679
Gene: GJB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 17019
ClinVar RCV Id: RCV000018545
dbSNP Id: rs104894407
MyVariant Identifiers: chr13:g.20763589C>G (hg19) chr13:g.20189450C>G (hg38)
PubMed: PMID:11298683 PMID:20301708 PMID:20854437
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.20189450C>G , CM000675.2:g.20189450C>G GRCh38
NC_000013.10:g.20763589C>G , CM000675.1:g.20763589C>G GRCh37
NC_000013.9:g.19661589C>G NCBI36
NG_008358.1:g.8526G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000382844.2:c.132G>C ENSP00000372295.1:p.Trp44Cys
ENST00000382848.5:c.132G>C MANE Select ENSP00000372299.4:p.Trp44Cys
ENST00000382844.1:c.132G>C ENSP00000372295.1:p.Trp44Cys
ENST00000382848.4:c.132G>C ENSP00000372299.4:p.Trp44Cys
NM_004004.5:c.132G>C NP_003995.2:p.Trp44Cys
XM_011535049.1:c.132G>C XP_011533351.1:p.Trp44Cys
XM_011535049.2:c.132G>C XP_011533351.1:p.Trp44Cys
NM_004004.6:c.132G>C MANE Select NP_003995.2:p.Trp44Cys
Search 100 bp 5'
Search 100 bp 3'