Canonical Allele Identifier: CA417248469

Linked Data

MyVariant Identifiers: chr1:g.35250441C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34784840C>G , CM000663.2:g.34784840C>G GRCh38
NC_000001.10:g.35250441C>G , CM000663.1:g.35250441C>G GRCh37
NC_000001.9:g.35023028C>G NCBI36
NG_008309.1:g.8652C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000373366.3:c.78C>G (GJB3) MANE Select ENSP00000362464.2:p.Ser26=
ENST00000373362.3:c.78C>G (GJB3) ENSP00000362460.3:p.Ser26=
ENST00000373366.2:c.78C>G (GJB3) ENSP00000362464.2:p.Ser26=
ENST00000426886.1:c.208-66431G>C (SMIM12) ENSP00000429902.1:n.208-66431G>C
NM_001005752.1:c.78C>G (GJB3) NP_001005752.1:p.Ser26=
NM_024009.2:c.78C>G (GJB3) NP_076872.1:p.Ser26=
XR_947179.1:n.1001+13531G>C
XR_001737967.1:n.1023+13531G>C
NM_024009.3:c.78C>G (GJB3) MANE Select NP_076872.1:p.Ser26=
NM_001005752.2:c.78C>G (GJB3) NP_001005752.1:p.Ser26=