Canonical Allele Identifier: CA483153904

Gene: GJB2

Linked Data

• MyVariant Identifiers: chr13:g.20763220C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.20189081C>G , CM000675.2:g.20189081C>G	GRCh38
NC_000013.10:g.20763220C>G , CM000675.1:g.20763220C>G	GRCh37
NC_000013.9:g.19661220C>G	NCBI36
NG_008358.1:g.8895G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000382844.2:c.501G>C	ENSP00000372295.1:p.Val167=
ENST00000382848.5:c.501G>C MANE Select	ENSP00000372299.4:p.Val167=
ENST00000382844.1:c.501G>C	ENSP00000372295.1:p.Val167=
ENST00000382848.4:c.501G>C	ENSP00000372299.4:p.Val167=
NM_004004.5:c.501G>C	NP_003995.2:p.Val167=
XM_011535049.1:c.501G>C	XP_011533351.1:p.Val167=
XM_011535049.2:c.501G>C	XP_011533351.1:p.Val167=
NM_004004.6:c.501G>C MANE Select	NP_003995.2:p.Val167=