Canonical Allele Identifier: CA2644768982

Linked Data

gnomAD v4: 1-34781661-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34781661C>A , CM000663.2:g.34781661C>A GRCh38
NC_000001.10:g.35247262C>A , CM000663.1:g.35247262C>A GRCh37
NC_000001.9:g.35019849C>A NCBI36
NG_008309.1:g.5473C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373366.3:c.-143C>A (GJB3) MANE Select ENSP00000362464.2:n.-143C>A
ENST00000373366.2:c.-143C>A (GJB3) ENSP00000362464.2:n.-143C>A
ENST00000426886.1:c.208-63252G>T (SMIM12) ENSP00000429902.1:n.208-63252G>T
NM_024009.2:c.-143C>A (GJB3) NP_076872.1:n.-143C>A
XR_947179.1:n.1001+16710G>T
XR_001737967.1:n.1023+16710G>T
NM_024009.3:c.-143C>A (GJB3) MANE Select NP_076872.1:n.-143C>A