Canonical Allele Identifier: CA417248413

Linked Data

dbSNP Id: rs1640071255
gnomAD v4: 1-34784792-G-A
MyVariant Identifiers: chr1:g.35250393G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34784792G>A , CM000663.2:g.34784792G>A GRCh38
NC_000001.10:g.35250393G>A , CM000663.1:g.35250393G>A GRCh37
NC_000001.9:g.35022980G>A NCBI36
NG_008309.1:g.8604G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373366.3:c.30G>A (GJB3) MANE Select ENSP00000362464.2:p.Leu10=
ENST00000373362.3:c.30G>A (GJB3) ENSP00000362460.3:p.Leu10=
ENST00000373366.2:c.30G>A (GJB3) ENSP00000362464.2:p.Leu10=
ENST00000426886.1:c.208-66383C>T (SMIM12) ENSP00000429902.1:n.208-66383C>T
NM_001005752.1:c.30G>A (GJB3) NP_001005752.1:p.Leu10=
NM_024009.2:c.30G>A (GJB3) NP_076872.1:p.Leu10=
XR_947179.1:n.1001+13579C>T
XR_001737967.1:n.1023+13579C>T
NM_024009.3:c.30G>A (GJB3) MANE Select NP_076872.1:p.Leu10=
NM_001005752.2:c.30G>A (GJB3) NP_001005752.1:p.Leu10=