Canonical Allele Identifier: CA423738748
Gene: GJC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.228345777T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.228158076T>G , CM000663.2:g.228158076T>G GRCh38
NC_000001.10:g.228345777T>G , CM000663.1:g.228345777T>G GRCh37
NC_000001.9:g.226412400T>G NCBI36
NG_011838.1:g.13225T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000366714.3:c.318T>G MANE Select ENSP00000355675.2:p.Ser106=
ENST00000366714.2:c.318T>G ENSP00000355675.2:p.Ser106=
NM_020435.3:c.318T>G NP_065168.2:p.Ser106=
NM_020435.4:c.318T>G MANE Select NP_065168.2:p.Ser106=