Canonical Allele Identifier: CA1000465545

Linked Data

dbSNP Id: rs1640011649
gnomAD v3: 1-34781666-G-C
gnomAD v4: 1-34781666-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34781666G>C , CM000663.2:g.34781666G>C GRCh38
NC_000001.10:g.35247267G>C , CM000663.1:g.35247267G>C GRCh37
NC_000001.9:g.35019854G>C NCBI36
NG_008309.1:g.5478G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373366.3:c.-138G>C (GJB3) MANE Select ENSP00000362464.2:n.-138G>C
ENST00000373366.2:c.-138G>C (GJB3) ENSP00000362464.2:n.-138G>C
ENST00000426886.1:c.208-63257C>G (SMIM12) ENSP00000429902.1:n.208-63257C>G
NM_024009.2:c.-138G>C (GJB3) NP_076872.1:n.-138G>C
XR_947179.1:n.1001+16705C>G
XR_001737967.1:n.1023+16705C>G
NM_024009.3:c.-138G>C (GJB3) MANE Select NP_076872.1:n.-138G>C