Canonical Allele Identifier: CA417248361
Gene: GJB4 HGNC NCBI
SMIM12 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.35227032C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34761431C>T , CM000663.2:g.34761431C>T GRCh38
NC_000001.10:g.35227032C>T , CM000663.1:g.35227032C>T GRCh37
NC_000001.9:g.34999619C>T NCBI36
NG_016243.1:g.6691C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000339480.3:c.177C>T (GJB4) MANE Select ENSP00000345868.1:p.Gly59=
ENST00000339480.1:c.177C>T (GJB4) ENSP00000345868.1:p.Gly59=
ENST00000426886.1:c.208-43022G>A (SMIM12) ENSP00000429902.1:n.208-43022G>A
NM_153212.2:c.177C>T (GJB4) NP_694944.1:p.Gly59=
XM_011540679.1:c.177C>T (GJB4) XP_011538981.1:p.Gly59=
XR_947179.1:n.1002-17982G>A
XM_011540679.2:c.177C>T (GJB4) XP_011538981.1:p.Gly59=
XR_001737967.1:n.1023+36940G>A
NM_153212.3:c.177C>T (GJB4) MANE Select NP_694944.1:p.Gly59=
Search 100 bp 5'
Search 100 bp 3'