Canonical Allele Identifier: CA1162031891

Linked Data

dbSNP Id: rs1640011744

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34781668T>C , CM000663.2:g.34781668T>C GRCh38
NC_000001.10:g.35247269T>C , CM000663.1:g.35247269T>C GRCh37
NC_000001.9:g.35019856T>C NCBI36
NG_008309.1:g.5480T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373366.3:c.-136T>C (GJB3) MANE Select ENSP00000362464.2:n.-136T>C
ENST00000373366.2:c.-136T>C (GJB3) ENSP00000362464.2:n.-136T>C
ENST00000426886.1:c.208-63259A>G (SMIM12) ENSP00000429902.1:n.208-63259A>G
NM_024009.2:c.-136T>C (GJB3) NP_076872.1:n.-136T>C
XR_947179.1:n.1001+16703A>G
XR_001737967.1:n.1023+16703A>G
NM_024009.3:c.-136T>C (GJB3) MANE Select NP_076872.1:n.-136T>C