Canonical Allele Identifier: CA482146827
Gene: ACADS HGNC NCBI

Linked Data

gnomAD v4: 12-120738661-G-A
MyVariant Identifiers: chr12:g.121176464G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120738661G>A , CM000674.2:g.120738661G>A GRCh38
NC_000012.11:g.121176464G>A , CM000674.1:g.121176464G>A GRCh37
NC_000012.10:g.119660847G>A NCBI36
NG_007991.1:g.17894G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.924G>A MANE Select ENSP00000242592.4:p.Gln308=
ENST00000242592.8:c.924G>A ENSP00000242592.4:p.Gln308=
ENST00000411593.2:c.912G>A ENSP00000401045.2:p.Gln304=
NM_000017.3:c.924G>A NP_000008.1:p.Gln308=
NM_001302554.1:c.912G>A NP_001289483.1:p.Gln304=
NM_000017.4:c.924G>A MANE Select NP_000008.1:p.Gln308=
NM_001302554.2:c.912G>A NP_001289483.1:p.Gln304=
Search 100 bp 5'
Search 100 bp 3'