Canonical Allele Identifier: CA244495411
Gene: ACADS HGNC NCBI

Linked Data

ClinVar Variation Id: 2162215
ClinVar RCV Id: RCV003091167
dbSNP Id: rs1015232355
gnomAD v2: 12-121177128-C-T
gnomAD v3: 12-120739325-C-T
gnomAD v4: 12-120739325-C-T
MyVariant Identifiers: chr12:g.121177128C>T (hg19) chr12:g.120739325C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120739325C>T , CM000674.2:g.120739325C>T GRCh38
NC_000012.11:g.121177128C>T , CM000674.1:g.121177128C>T GRCh37
NC_000012.10:g.119661511C>T NCBI36
NG_007991.1:g.18558C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000242592.9:c.1116C>T MANE Select ENSP00000242592.4:p.Tyr372=
ENST00000242592.8:c.1116C>T ENSP00000242592.4:p.Tyr372=
ENST00000411593.2:c.1104C>T ENSP00000401045.2:p.Tyr368=
NM_000017.3:c.1116C>T NP_000008.1:p.Tyr372=
NM_001302554.1:c.1104C>T NP_001289483.1:p.Tyr368=
NM_000017.4:c.1116C>T MANE Select NP_000008.1:p.Tyr372=
NM_001302554.2:c.1104C>T NP_001289483.1:p.Tyr368=
Search 100 bp 5'
Search 100 bp 3'