Canonical Allele Identifier: CA342222893
Gene: GJA8 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.147380126A>C (hg19) chr1:g.147907999A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.147907999A>C , CM000663.2:g.147907999A>C GRCh38
NC_000001.10:g.147380126A>C , CM000663.1:g.147380126A>C GRCh37
NC_000001.9:g.145846750A>C NCBI36
NG_016242.1:g.10181A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369235.2:c.44A>C MANE Select ENSP00000358238.1:p.Asn15Thr
ENST00000369235.1:c.44A>C ENSP00000358238.1:p.Asn15Thr
NM_005267.4:c.44A>C NP_005258.2:p.Asn15Thr
XM_011509416.1:c.44A>C XP_011507718.1:p.Asn15Thr
XM_011509417.1:c.44A>C XP_011507719.1:p.Asn15Thr
XM_011509417.2:c.44A>C XP_011507719.1:p.Asn15Thr
XR_002956281.1:n.959A>C
NM_005267.5:c.44A>C MANE Select NP_005258.2:p.Asn15Thr
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