Canonical Allele Identifier: CA483154276
Gene: GJB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.20763108G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.20188969G>A , CM000675.2:g.20188969G>A GRCh38
NC_000013.10:g.20763108G>A , CM000675.1:g.20763108G>A GRCh37
NC_000013.9:g.19661108G>A NCBI36
NG_008358.1:g.9007C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000382844.2:c.613C>T ENSP00000372295.1:p.Leu205=
ENST00000382848.5:c.613C>T MANE Select ENSP00000372299.4:p.Leu205=
ENST00000382844.1:c.613C>T ENSP00000372295.1:p.Leu205=
ENST00000382848.4:c.613C>T ENSP00000372299.4:p.Leu205=
NM_004004.5:c.613C>T NP_003995.2:p.Leu205=
XM_011535049.1:c.613C>T XP_011533351.1:p.Leu205=
XM_011535049.2:c.613C>T XP_011533351.1:p.Leu205=
NM_004004.6:c.613C>T MANE Select NP_003995.2:p.Leu205=