Canonical Allele Identifier: CA2644768956

Linked Data

gnomAD v4: 1-34781643-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34781643G>T , CM000663.2:g.34781643G>T GRCh38
NC_000001.10:g.35247244G>T , CM000663.1:g.35247244G>T GRCh37
NC_000001.9:g.35019831G>T NCBI36
NG_008309.1:g.5455G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373366.3:c.-161G>T (GJB3) MANE Select ENSP00000362464.2:n.-161G>T
ENST00000373366.2:c.-161G>T (GJB3) ENSP00000362464.2:n.-161G>T
ENST00000426886.1:c.208-63234C>A (SMIM12) ENSP00000429902.1:n.208-63234C>A
NM_024009.2:c.-161G>T (GJB3) NP_076872.1:n.-161G>T
XR_947179.1:n.1001+16728C>A
XR_001737967.1:n.1023+16728C>A
NM_024009.3:c.-161G>T (GJB3) MANE Select NP_076872.1:n.-161G>T