Canonical Allele Identifier: CA342223526
Gene: GJA8 HGNC NCBI

Linked Data

dbSNP Id: rs1651882492

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.147908160G>T , CM000663.2:g.147908160G>T GRCh38
NC_000001.10:g.147380287G>T , CM000663.1:g.147380287G>T GRCh37
NC_000001.9:g.145846911G>T NCBI36
NG_016242.1:g.10342G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369235.2:c.205G>T MANE Select ENSP00000358238.1:p.Ala69Ser
ENST00000369235.1:c.205G>T ENSP00000358238.1:p.Ala69Ser
NM_005267.4:c.205G>T NP_005258.2:p.Ala69Ser
XM_011509416.1:c.205G>T XP_011507718.1:p.Ala69Ser
XM_011509417.1:c.205G>T XP_011507719.1:p.Ala69Ser
XM_011509417.2:c.205G>T XP_011507719.1:p.Ala69Ser
XR_002956281.1:n.1120G>T
NM_005267.5:c.205G>T MANE Select NP_005258.2:p.Ala69Ser