Canonical Allele Identifier: CA339300165

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34761432T>A , CM000663.2:g.34761432T>A GRCh38
NC_000001.10:g.35227033T>A , CM000663.1:g.35227033T>A GRCh37
NC_000001.9:g.34999620T>A NCBI36
NG_016243.1:g.6692T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000339480.3:c.178T>A (GJB4) MANE Select ENSP00000345868.1:p.Cys60Ser
ENST00000339480.1:c.178T>A (GJB4) ENSP00000345868.1:p.Cys60Ser
ENST00000426886.1:c.208-43023A>T (SMIM12) ENSP00000429902.1:n.208-43023A>T
NM_153212.2:c.178T>A (GJB4) NP_694944.1:p.Cys60Ser
XM_011540679.1:c.178T>A (GJB4) XP_011538981.1:p.Cys60Ser
XR_947179.1:n.1002-17983A>T
XM_011540679.2:c.178T>A (GJB4) XP_011538981.1:p.Cys60Ser
XR_001737967.1:n.1023+36939A>T
NM_153212.3:c.178T>A (GJB4) MANE Select NP_694944.1:p.Cys60Ser