Canonical Allele Identifier: CA1162031857

Linked Data

dbSNP Id: rs1557658260

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34781601G>A , CM000663.2:g.34781601G>A GRCh38
NC_000001.10:g.35247202G>A , CM000663.1:g.35247202G>A GRCh37
NC_000001.9:g.35019789G>A NCBI36
NG_008309.1:g.5413G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373366.3:c.-203G>A (GJB3) MANE Select ENSP00000362464.2:n.-203G>A
ENST00000373366.2:c.-203G>A (GJB3) ENSP00000362464.2:n.-203G>A
ENST00000426886.1:c.208-63192C>T (SMIM12) ENSP00000429902.1:n.208-63192C>T
NM_024009.2:c.-203G>A (GJB3) NP_076872.1:n.-203G>A
XR_947179.1:n.1001+16770C>T
XR_001737967.1:n.1023+16770C>T
NM_024009.3:c.-203G>A (GJB3) MANE Select NP_076872.1:n.-203G>A