Canonical Allele Identifier: CA2077137569
Gene: GJB2 HGNC NCBI

Linked Data

dbSNP Id: rs1959047738

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.20187721A>G , CM000675.2:g.20187721A>G GRCh38
NC_000013.10:g.20761860A>G , CM000675.1:g.20761860A>G GRCh37
NC_000013.9:g.19659860A>G NCBI36
NG_008358.1:g.10255T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000382844.2:c.*1180T>C ENSP00000372295.1:n.*1180T>C
ENST00000382848.5:c.*1180T>C MANE Select ENSP00000372299.4:n.*1180T>C
ENST00000382844.1:c.*1180T>C ENSP00000372295.1:n.*1180T>C
ENST00000382848.4:c.*1180T>C ENSP00000372299.4:n.*1180T>C
NM_004004.5:c.*1180T>C NP_003995.2:n.*1180T>C
XM_011535049.1:c.*1180T>C XP_011533351.1:n.*1180T>C
XM_011535049.2:c.*1180T>C XP_011533351.1:n.*1180T>C
NM_004004.6:c.*1180T>C MANE Select NP_003995.2:n.*1180T>C