Canonical Allele Identifier: CA2644768948

Linked Data

gnomAD v4: 1-34781635-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34781635T>C , CM000663.2:g.34781635T>C GRCh38
NC_000001.10:g.35247236T>C , CM000663.1:g.35247236T>C GRCh37
NC_000001.9:g.35019823T>C NCBI36
NG_008309.1:g.5447T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373366.3:c.-169T>C (GJB3) MANE Select ENSP00000362464.2:n.-169T>C
ENST00000373366.2:c.-169T>C (GJB3) ENSP00000362464.2:n.-169T>C
ENST00000426886.1:c.208-63226A>G (SMIM12) ENSP00000429902.1:n.208-63226A>G
NM_024009.2:c.-169T>C (GJB3) NP_076872.1:n.-169T>C
XR_947179.1:n.1001+16736A>G
XR_001737967.1:n.1023+16736A>G
NM_024009.3:c.-169T>C (GJB3) MANE Select NP_076872.1:n.-169T>C