Canonical Allele Identifier: CA452133885
Gene: GJA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.121768389A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.121447243A>T , CM000668.2:g.121447243A>T GRCh38
NC_000006.11:g.121768389A>T , CM000668.1:g.121768389A>T GRCh37
NC_000006.10:g.121810088A>T NCBI36
NG_008308.1:g.16645A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000282561.4:c.396A>T MANE Select ENSP00000282561.3:p.Ile132=
ENST00000647564.1:c.396A>T ENSP00000497565.1:p.Ile132=
ENST00000649003.1:c.396A>T ENSP00000497283.1:p.Ile132=
ENST00000650427.1:c.396A>T ENSP00000497367.1:p.Ile132=
ENST00000282561.3:c.396A>T ENSP00000282561.3:p.Ile132=
NM_000165.4:c.396A>T NP_000156.1:p.Ile132=
NM_000165.5:c.396A>T MANE Select NP_000156.1:p.Ile132=
Search 100 bp 5'
Search 100 bp 3'