Canonical Allele Identifier: CA1199652701
Gene: GJA8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.147908234G= , CM000663.2:g.147908234G= GRCh38
NC_000001.10:g.147380361G= , CM000663.1:g.147380361G= GRCh37
NC_000001.9:g.145846985G= NCBI36
NG_016242.1:g.10416G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369235.2:c.279G= MANE Select ENSP00000358238.1:p.Val93=
ENST00000369235.1:c.279G= ENSP00000358238.1:p.Val93=
NM_005267.4:c.279G= NP_005258.2:p.Val93=
XM_011509416.1:c.279G= XP_011507718.1:p.Val93=
XM_011509417.1:c.279G= XP_011507719.1:p.Val93=
XM_011509417.2:c.279G= XP_011507719.1:p.Val93=
XR_002956281.1:n.1194G=
NM_005267.5:c.279G= MANE Select NP_005258.2:p.Val93=