Canonical Allele Identifier: CA2077114697
Gene: GJB2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.20192799C= , CM000675.2:g.20192799C= GRCh38
NC_000013.10:g.20766938C= , CM000675.1:g.20766938C= GRCh37
NC_000013.9:g.19664938C= NCBI36
NG_008358.1:g.5177G=

Transcript Alleles

HGVS Amino-acid change
ENST00000382848.5:c.-39G= MANE Select ENSP00000372299.4:n.-39G=
ENST00000382848.4:c.-39G= ENSP00000372299.4:n.-39G=
NM_004004.5:c.-39G= NP_003995.2:n.-39G=
NM_004004.6:c.-39G= MANE Select NP_003995.2:n.-39G=
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