Canonical Allele Identifier: CA2621371280

Gene: ACADS

Linked Data

• dbSNP Id: rs2136951537
• gnomAD v4: 12-120739677-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.120739677A>G , CM000674.2:g.120739677A>G	GRCh38
NC_000012.11:g.121177480A>G , CM000674.1:g.121177480A>G	GRCh37
NC_000012.10:g.119661863A>G	NCBI36
NG_007991.1:g.18910A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242592.9:c.*229A>G MANE Select	ENSP00000242592.4:n.*229A>G
ENST00000242592.8:c.*229A>G	ENSP00000242592.4:n.*229A>G
NM_000017.3:c.*229A>G	NP_000008.1:n.*229A>G
NM_001302554.1:c.*229A>G	NP_001289483.1:n.*229A>G
NM_000017.4:c.*229A>G MANE Select	NP_000008.1:n.*229A>G
NM_001302554.2:c.*229A>G	NP_001289483.1:n.*229A>G