Canonical Allele Identifier: CA420607101

Gene: GJA8

Linked Data

• MyVariant Identifiers: chr1:g.147380532C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.147908405C>G , CM000663.2:g.147908405C>G	GRCh38
NC_000001.10:g.147380532C>G , CM000663.1:g.147380532C>G	GRCh37
NC_000001.9:g.145847156C>G	NCBI36
NG_016242.1:g.10587C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369235.2:c.450C>G MANE Select	ENSP00000358238.1:p.Thr150=
ENST00000369235.1:c.450C>G	ENSP00000358238.1:p.Thr150=
NM_005267.4:c.450C>G	NP_005258.2:p.Thr150=
XM_011509416.1:c.450C>G	XP_011507718.1:p.Thr150=
XM_011509417.1:c.450C>G	XP_011507719.1:p.Thr150=
XM_011509417.2:c.450C>G	XP_011507719.1:p.Thr150=
XR_002956281.1:n.1365C>G
NM_005267.5:c.450C>G MANE Select	NP_005258.2:p.Thr150=