Canonical Allele Identifier: CA378615999
Gene: ACADSB HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.124793980T>A (hg19) chr10:g.123034464T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.123034464T>A , CM000672.2:g.123034464T>A GRCh38
NC_000010.10:g.124793980T>A , CM000672.1:g.124793980T>A GRCh37
NC_000010.9:g.124783970T>A NCBI36
NG_008003.1:g.30552T>A , LRG_451:g.30552T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000358776.7:c.151T>A MANE Select ENSP00000357873.3:p.Phe51Ile
ENST00000358776.6:c.151T>A ENSP00000357873.3:p.Phe51Ile
ENST00000368869.8:c.-55T>A ENSP00000357862.4:n.-55T>A
ENST00000411816.2:n.168T>A
NM_001609.3:c.151T>A , LRG_451t1:c.151T>A NP_001600.1:p.Phe51Ile
NM_001330174.1:c.-55T>A NP_001317103.1:n.-55T>A
NM_001330174.2:c.-55T>A NP_001317103.1:n.-55T>A
NM_001609.4:c.151T>A MANE Select NP_001600.1:p.Phe51Ile
NM_001330174.3:c.-55T>A NP_001317103.1:n.-55T>A
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