Canonical Allele Identifier: CA127013
Gene: GJA1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 16985
dbSNP Id: rs104893964

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.121446912G>A , CM000668.2:g.121446912G>A GRCh38
NC_000006.11:g.121768058G>A , CM000668.1:g.121768058G>A GRCh37
NC_000006.10:g.121809757G>A NCBI36
NG_008308.1:g.16314G>A

Transcript Alleles

HGVS Amino-acid change
NM_000165.4:c.65G>A VV NP_000156.1:p.Gly22Glu
NM_000165.5:c.65G>A VV
ENST00000282561.3:c.65G>A ENSP00000282561.3:p.Gly22Glu