Canonical Allele Identifier: CA339300827

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34761499T>A , CM000663.2:g.34761499T>A GRCh38
NC_000001.10:g.35227100T>A , CM000663.1:g.35227100T>A GRCh37
NC_000001.9:g.34999687T>A NCBI36
NG_016243.1:g.6759T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000339480.3:c.245T>A (GJB4) MANE Select ENSP00000345868.1:p.Ile82Asn
ENST00000339480.1:c.245T>A (GJB4) ENSP00000345868.1:p.Ile82Asn
ENST00000426886.1:c.208-43090A>T (SMIM12) ENSP00000429902.1:n.208-43090A>T
NM_153212.2:c.245T>A (GJB4) NP_694944.1:p.Ile82Asn
XM_011540679.1:c.245T>A (GJB4) XP_011538981.1:p.Ile82Asn
XR_947179.1:n.1002-18050A>T
XM_011540679.2:c.245T>A (GJB4) XP_011538981.1:p.Ile82Asn
XR_001737967.1:n.1023+36872A>T
NM_153212.3:c.245T>A (GJB4) MANE Select NP_694944.1:p.Ile82Asn