Canonical Allele Identifier: CA2696851618
Gene: GJA8 HGNC NCBI

Linked Data

dbSNP Id: rs1651859520

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.147907888T>A , CM000663.2:g.147907888T>A GRCh38
NC_000001.10:g.147380015T>A , CM000663.1:g.147380015T>A GRCh37
NC_000001.9:g.145846639T>A NCBI36
NG_016242.1:g.10070T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369235.2:c.-11-57T>A MANE Select ENSP00000358238.1:n.-11-57T>A
NM_005267.4:c.-11-57T>A NP_005258.2:n.-11-57T>A
XM_011509416.1:c.-68T>A XP_011507718.1:n.-68T>A
XM_011509417.1:c.-68T>A XP_011507719.1:n.-68T>A
XM_011509417.2:c.-68T>A XP_011507719.1:n.-68T>A
XR_002956281.1:n.848T>A
NM_005267.5:c.-11-57T>A MANE Select NP_005258.2:n.-11-57T>A