Canonical Allele Identifier: CA933372219
Gene: ACADSB HGNC NCBI

Linked Data

dbSNP Id: rs1850372426

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.123034580A>G , CM000672.2:g.123034580A>G GRCh38
NC_000010.10:g.124794096A>G , CM000672.1:g.124794096A>G GRCh37
NC_000010.9:g.124784086A>G NCBI36
NG_008003.1:g.30668A>G , LRG_451:g.30668A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000358776.7:c.202+65A>G MANE Select ENSP00000357873.3:n.202+65A>G
ENST00000358776.6:c.202+65A>G ENSP00000357873.3:n.202+65A>G
ENST00000368869.8:c.-4+65A>G ENSP00000357862.4:n.-4+65A>G
ENST00000411816.2:n.219+65A>G
NM_001609.3:c.202+65A>G , LRG_451t1:c.202+65A>G NP_001600.1:n.202+65A>G
NM_001330174.1:c.-4+65A>G NP_001317103.1:n.-4+65A>G
NM_001330174.2:c.-4+65A>G NP_001317103.1:n.-4+65A>G
NM_001609.4:c.202+65A>G MANE Select NP_001600.1:n.202+65A>G
NM_001330174.3:c.-4+65A>G NP_001317103.1:n.-4+65A>G