Canonical Allele Identifier: CA2789793316
Gene: ACADSB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.123052923A>G , CM000672.2:g.123052923A>G GRCh38
NC_000010.10:g.124812439A>G , CM000672.1:g.124812439A>G GRCh37
NC_000010.9:g.124802429A>G NCBI36
NG_008003.1:g.49011A>G , LRG_451:g.49011A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000358776.7:c.1129-138A>G MANE Select ENSP00000357873.3:n.1129-138A>G
ENST00000358776.6:c.1129-138A>G ENSP00000357873.3:n.1129-138A>G
ENST00000368869.8:c.823-138A>G ENSP00000357862.4:n.823-138A>G
ENST00000541070.1:n.163A>G
NM_001609.3:c.1129-138A>G , LRG_451t1:c.1129-138A>G NP_001600.1:n.1129-138A>G
NM_001330174.1:c.823-138A>G NP_001317103.1:n.823-138A>G
NM_001330174.2:c.823-138A>G NP_001317103.1:n.823-138A>G
NM_001609.4:c.1129-138A>G MANE Select NP_001600.1:n.1129-138A>G
NM_001330174.3:c.823-138A>G NP_001317103.1:n.823-138A>G
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