Canonical Allele Identifier: CA2067556035
Gene: ACADS HGNC NCBI

Linked Data

dbSNP Id: rs1883599197

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120739726C>G , CM000674.2:g.120739726C>G GRCh38
NC_000012.11:g.121177529C>G , CM000674.1:g.121177529C>G GRCh37
NC_000012.10:g.119661912C>G NCBI36
NG_007991.1:g.18959C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.*278C>G MANE Select ENSP00000242592.4:n.*278C>G
ENST00000242592.8:c.*278C>G ENSP00000242592.4:n.*278C>G
NM_000017.3:c.*278C>G NP_000008.1:n.*278C>G
NM_001302554.1:c.*278C>G NP_001289483.1:n.*278C>G
NM_000017.4:c.*278C>G MANE Select NP_000008.1:n.*278C>G
NM_001302554.2:c.*278C>G NP_001289483.1:n.*278C>G