Canonical Allele Identifier: CA1000465560

Linked Data

dbSNP Id: rs1557658298
gnomAD v3: 1-34781697-G-A
gnomAD v4: 1-34781697-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34781697G>A , CM000663.2:g.34781697G>A GRCh38
NC_000001.10:g.35247298G>A , CM000663.1:g.35247298G>A GRCh37
NC_000001.9:g.35019885G>A NCBI36
NG_008309.1:g.5509G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373366.3:c.-107G>A (GJB3) MANE Select ENSP00000362464.2:n.-107G>A
ENST00000373366.2:c.-107G>A (GJB3) ENSP00000362464.2:n.-107G>A
ENST00000426886.1:c.208-63288C>T (SMIM12) ENSP00000429902.1:n.208-63288C>T
NM_024009.2:c.-107G>A (GJB3) NP_076872.1:n.-107G>A
XR_947179.1:n.1001+16674C>T
XR_001737967.1:n.1023+16674C>T
NM_024009.3:c.-107G>A (GJB3) MANE Select NP_076872.1:n.-107G>A