Canonical Allele Identifier: CA339300478
Gene: GJB4 HGNC NCBI
SMIM12 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.35227060T>A (hg19) chr1:g.34761459T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34761459T>A , CM000663.2:g.34761459T>A GRCh38
NC_000001.10:g.35227060T>A , CM000663.1:g.35227060T>A GRCh37
NC_000001.9:g.34999647T>A NCBI36
NG_016243.1:g.6719T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000339480.3:c.205T>A (GJB4) MANE Select ENSP00000345868.1:p.Phe69Ile
ENST00000339480.1:c.205T>A (GJB4) ENSP00000345868.1:p.Phe69Ile
ENST00000426886.1:c.208-43050A>T (SMIM12) ENSP00000429902.1:n.208-43050A>T
NM_153212.2:c.205T>A (GJB4) NP_694944.1:p.Phe69Ile
XM_011540679.1:c.205T>A (GJB4) XP_011538981.1:p.Phe69Ile
XR_947179.1:n.1002-18010A>T
XM_011540679.2:c.205T>A (GJB4) XP_011538981.1:p.Phe69Ile
XR_001737967.1:n.1023+36912A>T
NM_153212.3:c.205T>A (GJB4) MANE Select NP_694944.1:p.Phe69Ile
Search 100 bp 5'
Search 100 bp 3'