Canonical Allele Identifier: CA1162023551

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34761410C= , CM000663.2:g.34761410C= GRCh38
NC_000001.10:g.35227011C= , CM000663.1:g.35227011C= GRCh37
NC_000001.9:g.34999598C= NCBI36
NG_016243.1:g.6670C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000339480.3:c.156C= (GJB4) MANE Select ENSP00000345868.1:p.Val52=
ENST00000339480.1:c.156C= (GJB4) ENSP00000345868.1:p.Val52=
ENST00000426886.1:c.208-43001G= (SMIM12) ENSP00000429902.1:n.208-43001G=
NM_153212.2:c.156C= (GJB4) NP_694944.1:p.Val52=
XM_011540679.1:c.156C= (GJB4) XP_011538981.1:p.Val52=
XR_947179.1:n.1002-17961G=
XM_011540679.2:c.156C= (GJB4) XP_011538981.1:p.Val52=
XR_001737967.1:n.1023+36961G=
NM_153212.3:c.156C= (GJB4) MANE Select NP_694944.1:p.Val52=