Canonical Allele Identifier: CA452134236
Gene: GJA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.121768200T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.121447054T>A , CM000668.2:g.121447054T>A GRCh38
NC_000006.11:g.121768200T>A , CM000668.1:g.121768200T>A GRCh37
NC_000006.10:g.121809899T>A NCBI36
NG_008308.1:g.16456T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282561.4:c.207T>A MANE Select ENSP00000282561.3:p.Ser69=
ENST00000647564.1:c.207T>A ENSP00000497565.1:p.Ser69=
ENST00000649003.1:c.207T>A ENSP00000497283.1:p.Ser69=
ENST00000650427.1:c.207T>A ENSP00000497367.1:p.Ser69=
ENST00000282561.3:c.207T>A ENSP00000282561.3:p.Ser69=
NM_000165.4:c.207T>A NP_000156.1:p.Ser69=
NM_000165.5:c.207T>A MANE Select NP_000156.1:p.Ser69=