Canonical Allele Identifier: CA6831238
Gene: ACADS HGNC NCBI

Linked Data

dbSNP Id: rs375931905
ExAC: 12:121177207 C / A
gnomAD v2: 12-121177207-C-A
gnomAD v3: 12-120739404-C-A
gnomAD v4: 12-120739404-C-A
MyVariant Identifiers: chr12:g.121177207C>A (hg19) chr12:g.120739404C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120739404C>A , CM000674.2:g.120739404C>A GRCh38
NC_000012.11:g.121177207C>A , CM000674.1:g.121177207C>A GRCh37
NC_000012.10:g.119661590C>A NCBI36
NG_007991.1:g.18637C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.1195C>A MANE Select ENSP00000242592.4:p.Arg399=
ENST00000242592.8:c.1195C>A ENSP00000242592.4:p.Arg399=
ENST00000411593.2:c.1183C>A ENSP00000401045.2:p.Arg395=
NM_000017.3:c.1195C>A NP_000008.1:p.Arg399=
NM_001302554.1:c.1183C>A NP_001289483.1:p.Arg395=
NM_000017.4:c.1195C>A MANE Select NP_000008.1:p.Arg399=
NM_001302554.2:c.1183C>A NP_001289483.1:p.Arg395=
Search 100 bp 5'
Search 100 bp 3'