Canonical Allele Identifier: CA420326662

Gene: GJA8

Linked Data

• MyVariant Identifiers: chr1:g.147380106G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.147907979G>T , CM000663.2:g.147907979G>T	GRCh38
NC_000001.10:g.147380106G>T , CM000663.1:g.147380106G>T	GRCh37
NC_000001.9:g.145846730G>T	NCBI36
NG_016242.1:g.10161G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369235.2:c.24G>T MANE Select	ENSP00000358238.1:p.Gly8=
ENST00000369235.1:c.24G>T	ENSP00000358238.1:p.Gly8=
NM_005267.4:c.24G>T	NP_005258.2:p.Gly8=
XM_011509416.1:c.24G>T	XP_011507718.1:p.Gly8=
XM_011509417.1:c.24G>T	XP_011507719.1:p.Gly8=
XM_011509417.2:c.24G>T	XP_011507719.1:p.Gly8=
XR_002956281.1:n.939G>T
NM_005267.5:c.24G>T MANE Select	NP_005258.2:p.Gly8=