Canonical Allele Identifier: CA339301386

Linked Data

gnomAD v4: 1-34761588-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34761588A>G , CM000663.2:g.34761588A>G GRCh38
NC_000001.10:g.35227189A>G , CM000663.1:g.35227189A>G GRCh37
NC_000001.9:g.34999776A>G NCBI36
NG_016243.1:g.6848A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000339480.3:c.334A>G (GJB4) MANE Select ENSP00000345868.1:p.Asn112Asp
ENST00000339480.1:c.334A>G (GJB4) ENSP00000345868.1:p.Asn112Asp
ENST00000426886.1:c.208-43179T>C (SMIM12) ENSP00000429902.1:n.208-43179T>C
NM_153212.2:c.334A>G (GJB4) NP_694944.1:p.Asn112Asp
XM_011540679.1:c.334A>G (GJB4) XP_011538981.1:p.Asn112Asp
XR_947179.1:n.1002-18139T>C
XM_011540679.2:c.334A>G (GJB4) XP_011538981.1:p.Asn112Asp
XR_001737967.1:n.1023+36783T>C
NM_153212.3:c.334A>G (GJB4) MANE Select NP_694944.1:p.Asn112Asp