Canonical Allele Identifier: CA20568557

Linked Data

dbSNP Id: rs965131230
gnomAD v2: 1-35247258-G-A
gnomAD v3: 1-34781657-G-A
gnomAD v4: 1-34781657-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34781657G>A , CM000663.2:g.34781657G>A GRCh38
NC_000001.10:g.35247258G>A , CM000663.1:g.35247258G>A GRCh37
NC_000001.9:g.35019845G>A NCBI36
NG_008309.1:g.5469G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373366.3:c.-147G>A (GJB3) MANE Select ENSP00000362464.2:n.-147G>A
ENST00000373366.2:c.-147G>A (GJB3) ENSP00000362464.2:n.-147G>A
ENST00000426886.1:c.208-63248C>T (SMIM12) ENSP00000429902.1:n.208-63248C>T
NM_024009.2:c.-147G>A (GJB3) NP_076872.1:n.-147G>A
XR_947179.1:n.1001+16714C>T
XR_001737967.1:n.1023+16714C>T
NM_024009.3:c.-147G>A (GJB3) MANE Select NP_076872.1:n.-147G>A