Canonical Allele Identifier: CA482146883
Gene: ACADS HGNC NCBI

Linked Data

gnomAD v4: 12-120739322-C-G
MyVariant Identifiers: chr12:g.121177125C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120739322C>G , CM000674.2:g.120739322C>G GRCh38
NC_000012.11:g.121177125C>G , CM000674.1:g.121177125C>G GRCh37
NC_000012.10:g.119661508C>G NCBI36
NG_007991.1:g.18555C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000242592.9:c.1113C>G MANE Select ENSP00000242592.4:p.Gly371=
ENST00000242592.8:c.1113C>G ENSP00000242592.4:p.Gly371=
ENST00000411593.2:c.1101C>G ENSP00000401045.2:p.Gly367=
NM_000017.3:c.1113C>G NP_000008.1:p.Gly371=
NM_001302554.1:c.1101C>G NP_001289483.1:p.Gly367=
NM_000017.4:c.1113C>G MANE Select NP_000008.1:p.Gly371=
NM_001302554.2:c.1101C>G NP_001289483.1:p.Gly367=
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