Canonical Allele Identifier: CA696361440
Gene: GJB2 HGNC NCBI

Linked Data

dbSNP Id: rs1458761526
MyVariant Identifiers: chr13:g.20762077C>G (hg19) chr13:g.20187938C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.20187938C>G , CM000675.2:g.20187938C>G GRCh38
NC_000013.10:g.20762077C>G , CM000675.1:g.20762077C>G GRCh37
NC_000013.9:g.19660077C>G NCBI36
NG_008358.1:g.10038G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000382844.2:c.*963G>C ENSP00000372295.1:n.*963G>C
ENST00000382848.5:c.*963G>C MANE Select ENSP00000372299.4:n.*963G>C
ENST00000382844.1:c.*963G>C ENSP00000372295.1:n.*963G>C
ENST00000382848.4:c.*963G>C ENSP00000372299.4:n.*963G>C
NM_004004.5:c.*963G>C NP_003995.2:n.*963G>C
XM_011535049.1:c.*963G>C XP_011533351.1:n.*963G>C
XM_011535049.2:c.*963G>C XP_011533351.1:n.*963G>C
NM_004004.6:c.*963G>C MANE Select NP_003995.2:n.*963G>C
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