Canonical Allele Identifier: CA452133983
Gene: GJA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.121768074A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.121446928A>C , CM000668.2:g.121446928A>C GRCh38
NC_000006.11:g.121768074A>C , CM000668.1:g.121768074A>C GRCh37
NC_000006.10:g.121809773A>C NCBI36
NG_008308.1:g.16330A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000282561.4:c.81A>C MANE Select ENSP00000282561.3:p.Ser27=
ENST00000647564.1:c.81A>C ENSP00000497565.1:p.Ser27=
ENST00000649003.1:c.81A>C ENSP00000497283.1:p.Ser27=
ENST00000650427.1:c.81A>C ENSP00000497367.1:p.Ser27=
ENST00000282561.3:c.81A>C ENSP00000282561.3:p.Ser27=
NM_000165.4:c.81A>C NP_000156.1:p.Ser27=
NM_000165.5:c.81A>C MANE Select NP_000156.1:p.Ser27=