Canonical Allele Identifier: CA127020
Gene: GJA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16997
dbSNP Id: rs267606845

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.121447073C>A , CM000668.2:g.121447073C>A GRCh38
NC_000006.11:g.121768219C>A , CM000668.1:g.121768219C>A GRCh37
NC_000006.10:g.121809918C>A NCBI36
NG_008308.1:g.16475C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282561.4:c.226C>A MANE Select ENSP00000282561.3:p.Arg76Ser
ENST00000647564.1:c.226C>A ENSP00000497565.1:p.Arg76Ser
ENST00000649003.1:c.226C>A ENSP00000497283.1:p.Arg76Ser
ENST00000650427.1:c.226C>A ENSP00000497367.1:p.Arg76Ser
ENST00000282561.3:c.226C>A ENSP00000282561.3:p.Arg76Ser
NM_000165.4:c.226C>A NP_000156.1:p.Arg76Ser
NM_000165.5:c.226C>A MANE Select NP_000156.1:p.Arg76Ser