Canonical Allele Identifier: CA1941711166
Gene: ACADSB HGNC NCBI

Linked Data

dbSNP Id: rs1850365473
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.123034201C>A , CM000672.2:g.123034201C>A GRCh38
NC_000010.10:g.124793717C>A , CM000672.1:g.124793717C>A GRCh37
NC_000010.9:g.124783707C>A NCBI36
NG_008003.1:g.30289C>A , LRG_451:g.30289C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000358776.7:c.43-155C>A MANE Select ENSP00000357873.3:n.43-155C>A
ENST00000358776.6:c.43-155C>A ENSP00000357873.3:n.43-155C>A
ENST00000368869.8:c.-163-155C>A ENSP00000357862.4:n.-163-155C>A
ENST00000411816.2:n.60-155C>A
NM_001609.3:c.43-155C>A , LRG_451t1:c.43-155C>A NP_001600.1:n.43-155C>A
NM_001330174.1:c.-163-155C>A NP_001317103.1:n.-163-155C>A
NM_001330174.2:c.-163-155C>A NP_001317103.1:n.-163-155C>A
NM_001609.4:c.43-155C>A MANE Select NP_001600.1:n.43-155C>A
NM_001330174.3:c.-163-155C>A NP_001317103.1:n.-163-155C>A
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