Canonical Allele Identifier: CA1430807
Gene: GJC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 261256
dbSNP Id: rs139992251

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.228157905C>T , CM000663.2:g.228157905C>T GRCh38
NC_000001.10:g.228345606C>T , CM000663.1:g.228345606C>T GRCh37
NC_000001.9:g.226412229C>T NCBI36
NG_011838.1:g.13054C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000366714.3:c.147C>T MANE Select ENSP00000355675.2:p.Asp49=
ENST00000366714.2:c.147C>T ENSP00000355675.2:p.Asp49=
NM_020435.3:c.147C>T NP_065168.2:p.Asp49=
NM_020435.4:c.147C>T MANE Select NP_065168.2:p.Asp49=