Canonical Allele Identifier: CA342224485
Gene: GJA8 HGNC NCBI

Linked Data

dbSNP Id: rs1651904718
MyVariant Identifiers: chr1:g.147380531C>A (hg19) chr1:g.147908404C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.147908404C>A , CM000663.2:g.147908404C>A GRCh38
NC_000001.10:g.147380531C>A , CM000663.1:g.147380531C>A GRCh37
NC_000001.9:g.145847155C>A NCBI36
NG_016242.1:g.10586C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369235.2:c.449C>A MANE Select ENSP00000358238.1:p.Thr150Asn
ENST00000369235.1:c.449C>A ENSP00000358238.1:p.Thr150Asn
NM_005267.4:c.449C>A NP_005258.2:p.Thr150Asn
XM_011509416.1:c.449C>A XP_011507718.1:p.Thr150Asn
XM_011509417.1:c.449C>A XP_011507719.1:p.Thr150Asn
XM_011509417.2:c.449C>A XP_011507719.1:p.Thr150Asn
XR_002956281.1:n.1364C>A
NM_005267.5:c.449C>A MANE Select NP_005258.2:p.Thr150Asn
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