Canonical Allele Identifier: CA378615581
Gene: ACADSB HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.124793877A>T (hg19) chr10:g.123034361A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.123034361A>T , CM000672.2:g.123034361A>T GRCh38
NC_000010.10:g.124793877A>T , CM000672.1:g.124793877A>T GRCh37
NC_000010.9:g.124783867A>T NCBI36
NG_008003.1:g.30449A>T , LRG_451:g.30449A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000358776.7:c.48A>T MANE Select ENSP00000357873.3:p.Arg16Ser
ENST00000358776.6:c.48A>T ENSP00000357873.3:p.Arg16Ser
ENST00000368869.8:c.-158A>T ENSP00000357862.4:n.-158A>T
ENST00000411816.2:n.65A>T
NM_001609.3:c.48A>T , LRG_451t1:c.48A>T NP_001600.1:p.Arg16Ser
NM_001330174.1:c.-158A>T NP_001317103.1:n.-158A>T
NM_001330174.2:c.-158A>T NP_001317103.1:n.-158A>T
NM_001609.4:c.48A>T MANE Select NP_001600.1:p.Arg16Ser
NM_001330174.3:c.-158A>T NP_001317103.1:n.-158A>T
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