Canonical Allele Identifier: CA386601396
Gene: ACADS HGNC NCBI

Linked Data

gnomAD v4: 12-120738669-A-G
MyVariant Identifiers: chr12:g.121176472A>G (hg19) chr12:g.120738669A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120738669A>G , CM000674.2:g.120738669A>G GRCh38
NC_000012.11:g.121176472A>G , CM000674.1:g.121176472A>G GRCh37
NC_000012.10:g.119660855A>G NCBI36
NG_007991.1:g.17902A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.932A>G MANE Select ENSP00000242592.4:p.Gln311Arg
ENST00000242592.8:c.932A>G ENSP00000242592.4:p.Gln311Arg
ENST00000411593.2:c.920A>G ENSP00000401045.2:p.Gln307Arg
NM_000017.3:c.932A>G NP_000008.1:p.Gln311Arg
NM_001302554.1:c.920A>G NP_001289483.1:p.Gln307Arg
NM_000017.4:c.932A>G MANE Select NP_000008.1:p.Gln311Arg
NM_001302554.2:c.920A>G NP_001289483.1:p.Gln307Arg
Search 100 bp 5'
Search 100 bp 3'