Canonical Allele Identifier: CA10631099
Gene: ACADSB HGNC NCBI

Linked Data

ClinVar Variation Id: 299062
ClinVar RCV Id: RCV000363948
dbSNP Id: rs886046775
gnomAD v4: 10-123008928-G-C
MyVariant Identifiers: chr10:g.124768444G>C (hg19) chr10:g.123008928G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.123008928G>C , CM000672.2:g.123008928G>C GRCh38
NC_000010.10:g.124768444G>C , CM000672.1:g.124768444G>C GRCh37
NC_000010.9:g.124758434G>C NCBI36
NG_008003.1:g.5016G>C , LRG_451:g.5016G>C
NG_067239.1:g.4868C>G

Transcript Alleles

HGVS Amino-acid Change
NM_001609.3:c.-102G>C , LRG_451t1:c.-102G>C NP_001600.1:n.-102G>C
NM_001330174.1:c.-307G>C NP_001317103.1:n.-307G>C
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