Canonical Allele Identifier: CA10641619
Gene: ACTC1 HGNC NCBI
GJD2-DT HGNC NCBI

Linked Data

ClinVar Variation Id: 315675
ClinVar RCV Id: RCV000269922 RCV000365397
dbSNP Id: rs886051073
gnomAD v3: 15-34789547-A-G
gnomAD v4: 15-34789547-A-G
MyVariant Identifiers: chr15:g.35081748A>G (hg19) chr15:g.34789547A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.34789547A>G , CM000677.2:g.34789547A>G GRCh38
NC_000015.9:g.35081748A>G , CM000677.1:g.35081748A>G GRCh37
NC_000015.8:g.32869040A>G NCBI36
NG_007553.1:g.11180T>C , LRG_388:g.11180T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000290378.4:c.*865T>C (ACTC1) ENSP00000290378.4:n.*865T>C
NM_005159.4:c.*865T>C , LRG_388t1:c.*865T>C (ACTC1) NP_005150.1:n.*865T>C
NR_120329.1:n.299+12116A>G (GJD2-DT)
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