Canonical Allele Identifier: CA1941711386
Gene: ACADSB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.123034725G= , CM000672.2:g.123034725G= GRCh38
NC_000010.10:g.124794241G= , CM000672.1:g.124794241G= GRCh37
NC_000010.9:g.124784231G= NCBI36
NG_008003.1:g.30813G= , LRG_451:g.30813G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000358776.7:c.202+210G= MANE Select ENSP00000357873.3:n.202+210G=
ENST00000358776.6:c.202+210G= ENSP00000357873.3:n.202+210G=
ENST00000368869.8:c.-4+210G= ENSP00000357862.4:n.-4+210G=
ENST00000411816.2:n.219+210G=
NM_001609.3:c.202+210G= , LRG_451t1:c.202+210G= NP_001600.1:n.202+210G=
NM_001330174.1:c.-4+210G= NP_001317103.1:n.-4+210G=
NM_001330174.2:c.-4+210G= NP_001317103.1:n.-4+210G=
NM_001609.4:c.202+210G= MANE Select NP_001600.1:n.202+210G=
NM_001330174.3:c.-4+210G= NP_001317103.1:n.-4+210G=
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