Canonical Allele Identifier: CA378615674
Gene: ACADSB HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.124793905T>C (hg19) chr10:g.123034389T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.123034389T>C , CM000672.2:g.123034389T>C GRCh38
NC_000010.10:g.124793905T>C , CM000672.1:g.124793905T>C GRCh37
NC_000010.9:g.124783895T>C NCBI36
NG_008003.1:g.30477T>C , LRG_451:g.30477T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000358776.7:c.76T>C MANE Select ENSP00000357873.3:p.Trp26Arg
ENST00000358776.6:c.76T>C ENSP00000357873.3:p.Trp26Arg
ENST00000368869.8:c.-130T>C ENSP00000357862.4:n.-130T>C
ENST00000411816.2:n.93T>C
NM_001609.3:c.76T>C , LRG_451t1:c.76T>C NP_001600.1:p.Trp26Arg
NM_001330174.1:c.-130T>C NP_001317103.1:n.-130T>C
NM_001330174.2:c.-130T>C NP_001317103.1:n.-130T>C
NM_001609.4:c.76T>C MANE Select NP_001600.1:p.Trp26Arg
NM_001330174.3:c.-130T>C NP_001317103.1:n.-130T>C
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