Canonical Allele Identifier: CA452134373
Gene: GJA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.121768257C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.121447111C>G , CM000668.2:g.121447111C>G GRCh38
NC_000006.11:g.121768257C>G , CM000668.1:g.121768257C>G GRCh37
NC_000006.10:g.121809956C>G NCBI36
NG_008308.1:g.16513C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282561.4:c.264C>G MANE Select ENSP00000282561.3:p.Pro88=
ENST00000647564.1:c.264C>G ENSP00000497565.1:p.Pro88=
ENST00000649003.1:c.264C>G ENSP00000497283.1:p.Pro88=
ENST00000650427.1:c.264C>G ENSP00000497367.1:p.Pro88=
ENST00000282561.3:c.264C>G ENSP00000282561.3:p.Pro88=
NM_000165.4:c.264C>G NP_000156.1:p.Pro88=
NM_000165.5:c.264C>G MANE Select NP_000156.1:p.Pro88=