Canonical Allele Identifier: CA6904238
Gene: GJB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 882640
ClinVar RCV Id: RCV001112459 RCV001112460 RCV001112458
dbSNP Id: rs753674300
ExAC: 13:20763164 G / A
gnomAD v2: 13-20763164-G-A
gnomAD v3: 13-20189025-G-A
gnomAD v4: 13-20189025-G-A
MyVariant Identifiers: chr13:g.20763164G>A (hg19) chr13:g.20189025G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.20189025G>A , CM000675.2:g.20189025G>A GRCh38
NC_000013.10:g.20763164G>A , CM000675.1:g.20763164G>A GRCh37
NC_000013.9:g.19661164G>A NCBI36
NG_008358.1:g.8951C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382844.2:c.557C>T ENSP00000372295.1:p.Thr186Met
ENST00000382848.5:c.557C>T MANE Select ENSP00000372299.4:p.Thr186Met
ENST00000382844.1:c.557C>T ENSP00000372295.1:p.Thr186Met
ENST00000382848.4:c.557C>T ENSP00000372299.4:p.Thr186Met
NM_004004.5:c.557C>T NP_003995.2:p.Thr186Met
XM_011535049.1:c.557C>T XP_011533351.1:p.Thr186Met
XM_011535049.2:c.557C>T XP_011533351.1:p.Thr186Met
NM_004004.6:c.557C>T MANE Select NP_003995.2:p.Thr186Met
Search 100 bp 5'
Search 100 bp 3'