Canonical Allele Identifier: CA2644768929

Linked Data

gnomAD v4: 1-34781613-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34781613A>G , CM000663.2:g.34781613A>G GRCh38
NC_000001.10:g.35247214A>G , CM000663.1:g.35247214A>G GRCh37
NC_000001.9:g.35019801A>G NCBI36
NG_008309.1:g.5425A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000373366.3:c.-191A>G (GJB3) MANE Select ENSP00000362464.2:n.-191A>G
ENST00000373366.2:c.-191A>G (GJB3) ENSP00000362464.2:n.-191A>G
ENST00000426886.1:c.208-63204T>C (SMIM12) ENSP00000429902.1:n.208-63204T>C
NM_024009.2:c.-191A>G (GJB3) NP_076872.1:n.-191A>G
XR_947179.1:n.1001+16758T>C
XR_001737967.1:n.1023+16758T>C
NM_024009.3:c.-191A>G (GJB3) MANE Select NP_076872.1:n.-191A>G