Canonical Allele Identifier: CA365557865
Gene: GJA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.121768069C>A (hg19) chr6:g.121446923C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.121446923C>A , CM000668.2:g.121446923C>A GRCh38
NC_000006.11:g.121768069C>A , CM000668.1:g.121768069C>A GRCh37
NC_000006.10:g.121809768C>A NCBI36
NG_008308.1:g.16325C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282561.4:c.76C>A MANE Select ENSP00000282561.3:p.Leu26Met
ENST00000647564.1:c.76C>A ENSP00000497565.1:p.Leu26Met
ENST00000649003.1:c.76C>A ENSP00000497283.1:p.Leu26Met
ENST00000650427.1:c.76C>A ENSP00000497367.1:p.Leu26Met
ENST00000282561.3:c.76C>A ENSP00000282561.3:p.Leu26Met
NM_000165.4:c.76C>A NP_000156.1:p.Leu26Met
NM_000165.5:c.76C>A MANE Select NP_000156.1:p.Leu26Met
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