Canonical Allele Identifier: CA339300394

Linked Data

dbSNP Id: rs200060483
gnomAD v3: 1-34761452-C-G
gnomAD v4: 1-34761452-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34761452C>G , CM000663.2:g.34761452C>G GRCh38
NC_000001.10:g.35227053C>G , CM000663.1:g.35227053C>G GRCh37
NC_000001.9:g.34999640C>G NCBI36
NG_016243.1:g.6712C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000339480.3:c.198C>G (GJB4) MANE Select ENSP00000345868.1:p.Asp66Glu
ENST00000339480.1:c.198C>G (GJB4) ENSP00000345868.1:p.Asp66Glu
ENST00000426886.1:c.208-43043G>C (SMIM12) ENSP00000429902.1:n.208-43043G>C
NM_153212.2:c.198C>G (GJB4) NP_694944.1:p.Asp66Glu
XM_011540679.1:c.198C>G (GJB4) XP_011538981.1:p.Asp66Glu
XR_947179.1:n.1002-18003G>C
XM_011540679.2:c.198C>G (GJB4) XP_011538981.1:p.Asp66Glu
XR_001737967.1:n.1023+36919G>C
NM_153212.3:c.198C>G (GJB4) MANE Select NP_694944.1:p.Asp66Glu