Canonical Allele Identifier: CA387460849
Gene: GJB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 438620
dbSNP Id: rs1378679640

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.20188998A>G , CM000675.2:g.20188998A>G GRCh38
NC_000013.10:g.20763137A>G , CM000675.1:g.20763137A>G GRCh37
NC_000013.9:g.19661137A>G NCBI36
NG_008358.1:g.8978T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000382844.2:c.584T>C ENSP00000372295.1:p.Met195Thr
ENST00000382848.5:c.584T>C MANE Select ENSP00000372299.4:p.Met195Thr
ENST00000382844.1:c.584T>C ENSP00000372295.1:p.Met195Thr
ENST00000382848.4:c.584T>C ENSP00000372299.4:p.Met195Thr
NM_004004.5:c.584T>C NP_003995.2:p.Met195Thr
XM_011535049.1:c.584T>C XP_011533351.1:p.Met195Thr
XM_011535049.2:c.584T>C XP_011533351.1:p.Met195Thr
NM_004004.6:c.584T>C MANE Select NP_003995.2:p.Met195Thr