Canonical Allele Identifier: CA1162031847

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34781595G= , CM000663.2:g.34781595G= GRCh38
NC_000001.10:g.35247196G= , CM000663.1:g.35247196G= GRCh37
NC_000001.9:g.35019783G= NCBI36
NG_008309.1:g.5407G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373366.3:c.-209G= (GJB3) MANE Select ENSP00000362464.2:n.-209G=
ENST00000373366.2:c.-209G= (GJB3) ENSP00000362464.2:n.-209G=
ENST00000426886.1:c.208-63186C= (SMIM12) ENSP00000429902.1:n.208-63186C=
NM_024009.2:c.-209G= (GJB3) NP_076872.1:n.-209G=
XR_947179.1:n.1001+16776C=
XR_001737967.1:n.1023+16776C=
NM_024009.3:c.-209G= (GJB3) MANE Select NP_076872.1:n.-209G=