Canonical Allele Identifier: CA483154037

Gene: GJB2

Linked Data

• dbSNP Id: rs1451806753
• MyVariant Identifiers: chr13:g.20763676T>C (hg19) ; chr13:g.20189537T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.20189537T>C , CM000675.2:g.20189537T>C	GRCh38
NC_000013.10:g.20763676T>C , CM000675.1:g.20763676T>C	GRCh37
NC_000013.9:g.19661676T>C	NCBI36
NG_008358.1:g.8439A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000382844.2:c.45A>G	ENSP00000372295.1:p.Lys15=
ENST00000382848.5:c.45A>G MANE Select	ENSP00000372299.4:p.Lys15=
ENST00000382844.1:c.45A>G	ENSP00000372295.1:p.Lys15=
ENST00000382848.4:c.45A>G	ENSP00000372299.4:p.Lys15=
NM_004004.5:c.45A>G	NP_003995.2:p.Lys15=
XM_011535049.1:c.45A>G	XP_011533351.1:p.Lys15=
XM_011535049.2:c.45A>G	XP_011533351.1:p.Lys15=
NM_004004.6:c.45A>G MANE Select	NP_003995.2:p.Lys15=