Canonical Allele Identifier: CA387461767
Gene: GJB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1297075
ClinVar RCV Id: RCV002051744
dbSNP Id: rs1555341986
MyVariant Identifiers: chr13:g.20763564A>T (hg19) chr13:g.20189425A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.20189425A>T , CM000675.2:g.20189425A>T GRCh38
NC_000013.10:g.20763564A>T , CM000675.1:g.20763564A>T GRCh37
NC_000013.9:g.19661564A>T NCBI36
NG_008358.1:g.8551T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382844.2:c.157T>A ENSP00000372295.1:p.Cys53Ser
ENST00000382848.5:c.157T>A MANE Select ENSP00000372299.4:p.Cys53Ser
ENST00000382844.1:c.157T>A ENSP00000372295.1:p.Cys53Ser
ENST00000382848.4:c.157T>A ENSP00000372299.4:p.Cys53Ser
NM_004004.5:c.157T>A NP_003995.2:p.Cys53Ser
XM_011535049.1:c.157T>A XP_011533351.1:p.Cys53Ser
XM_011535049.2:c.157T>A XP_011533351.1:p.Cys53Ser
NM_004004.6:c.157T>A MANE Select NP_003995.2:p.Cys53Ser
Search 100 bp 5'
Search 100 bp 3'