Canonical Allele Identifier: CA471754538
Gene: ACADSB HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.124793997A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.123034481A>C , CM000672.2:g.123034481A>C GRCh38
NC_000010.10:g.124793997A>C , CM000672.1:g.124793997A>C GRCh37
NC_000010.9:g.124783987A>C NCBI36
NG_008003.1:g.30569A>C , LRG_451:g.30569A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000358776.7:c.168A>C MANE Select ENSP00000357873.3:p.Thr56=
ENST00000358776.6:c.168A>C ENSP00000357873.3:p.Thr56=
ENST00000368869.8:c.-38A>C ENSP00000357862.4:n.-38A>C
ENST00000411816.2:n.185A>C
NM_001609.3:c.168A>C , LRG_451t1:c.168A>C NP_001600.1:p.Thr56=
NM_001330174.1:c.-38A>C NP_001317103.1:n.-38A>C
NM_001330174.2:c.-38A>C NP_001317103.1:n.-38A>C
NM_001609.4:c.168A>C MANE Select NP_001600.1:p.Thr56=
NM_001330174.3:c.-38A>C NP_001317103.1:n.-38A>C
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