Canonical Allele Identifier: CA134957
Gene: GJB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 44733
dbSNP Id: rs397516871

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.20189303C>T , CM000675.2:g.20189303C>T GRCh38
NC_000013.10:g.20763442C>T , CM000675.1:g.20763442C>T GRCh37
NC_000013.9:g.19661442C>T NCBI36
NG_008358.1:g.8673G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382844.2:c.279G>A ENSP00000372295.1:p.Met93Ile
ENST00000382848.5:c.279G>A MANE Select ENSP00000372299.4:p.Met93Ile
ENST00000382844.1:c.279G>A ENSP00000372295.1:p.Met93Ile
ENST00000382848.4:c.279G>A ENSP00000372299.4:p.Met93Ile
NM_004004.5:c.279G>A NP_003995.2:p.Met93Ile
XM_011535049.1:c.279G>A XP_011533351.1:p.Met93Ile
XM_011535049.2:c.279G>A XP_011533351.1:p.Met93Ile
NM_004004.6:c.279G>A MANE Select NP_003995.2:p.Met93Ile