Canonical Allele Identifier: CA2644768913

Linked Data

gnomAD v4: 1-34781593-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34781593C>T , CM000663.2:g.34781593C>T GRCh38
NC_000001.10:g.35247194C>T , CM000663.1:g.35247194C>T GRCh37
NC_000001.9:g.35019781C>T NCBI36
NG_008309.1:g.5405C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373366.3:c.-211C>T (GJB3) MANE Select ENSP00000362464.2:n.-211C>T
ENST00000373366.2:c.-211C>T (GJB3) ENSP00000362464.2:n.-211C>T
ENST00000426886.1:c.208-63184G>A (SMIM12) ENSP00000429902.1:n.208-63184G>A
NM_024009.2:c.-211C>T (GJB3) NP_076872.1:n.-211C>T
XR_947179.1:n.1001+16778G>A
XR_001737967.1:n.1023+16778G>A
NM_024009.3:c.-211C>T (GJB3) MANE Select NP_076872.1:n.-211C>T