Canonical Allele Identifier: CA339310278

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34784781C>T , CM000663.2:g.34784781C>T GRCh38
NC_000001.10:g.35250382C>T , CM000663.1:g.35250382C>T GRCh37
NC_000001.9:g.35022969C>T NCBI36
NG_008309.1:g.8593C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373366.3:c.19C>T (GJB3) MANE Select ENSP00000362464.2:p.Gln7Ter
ENST00000373362.3:c.19C>T (GJB3) ENSP00000362460.3:p.Gln7Ter
ENST00000373366.2:c.19C>T (GJB3) ENSP00000362464.2:p.Gln7Ter
ENST00000426886.1:c.208-66372G>A (SMIM12) ENSP00000429902.1:n.208-66372G>A
NM_001005752.1:c.19C>T (GJB3) NP_001005752.1:p.Gln7Ter
NM_024009.2:c.19C>T (GJB3) NP_076872.1:p.Gln7Ter
XR_947179.1:n.1001+13590G>A
XR_001737967.1:n.1023+13590G>A
NM_024009.3:c.19C>T (GJB3) MANE Select NP_076872.1:p.Gln7Ter
NM_001005752.2:c.19C>T (GJB3) NP_001005752.1:p.Gln7Ter