Canonical Allele Identifier: CA246459534
Gene: GJB2 HGNC NCBI

Linked Data

dbSNP Id: rs1037871655
gnomAD v3: 13-20188765-G-C
gnomAD v4: 13-20188765-G-C
MyVariant Identifiers: chr13:g.20762904G>C (hg19) chr13:g.20188765G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.20188765G>C , CM000675.2:g.20188765G>C GRCh38
NC_000013.10:g.20762904G>C , CM000675.1:g.20762904G>C GRCh37
NC_000013.9:g.19660904G>C NCBI36
NG_008358.1:g.9211C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382844.2:c.*136C>G ENSP00000372295.1:n.*136C>G
ENST00000382848.5:c.*136C>G MANE Select ENSP00000372299.4:n.*136C>G
ENST00000382844.1:c.*136C>G ENSP00000372295.1:n.*136C>G
ENST00000382848.4:c.*136C>G ENSP00000372299.4:n.*136C>G
NM_004004.5:c.*136C>G NP_003995.2:n.*136C>G
XM_011535049.1:c.*136C>G XP_011533351.1:n.*136C>G
XM_011535049.2:c.*136C>G XP_011533351.1:n.*136C>G
NM_004004.6:c.*136C>G MANE Select NP_003995.2:n.*136C>G
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