Canonical Allele Identifier: CA607880669
Gene: ACADS HGNC NCBI

Linked Data

dbSNP Id: rs1255951402
gnomAD v2: 12-121174761-A-G
MyVariant Identifiers: chr12:g.121174761A>G (hg19) chr12:g.120736958A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120736958A>G , CM000674.2:g.120736958A>G GRCh38
NC_000012.11:g.121174761A>G , CM000674.1:g.121174761A>G GRCh37
NC_000012.10:g.119659144A>G NCBI36
NG_007991.1:g.16191A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000242592.9:c.211-28A>G MANE Select ENSP00000242592.4:n.211-28A>G
ENST00000242592.8:c.211-28A>G ENSP00000242592.4:n.211-28A>G
ENST00000411593.2:c.211-28A>G ENSP00000401045.2:n.211-28A>G
ENST00000539690.1:n.323-28A>G
NM_000017.3:c.211-28A>G NP_000008.1:n.211-28A>G
NM_001302554.1:c.211-28A>G NP_001289483.1:n.211-28A>G
NM_000017.4:c.211-28A>G MANE Select NP_000008.1:n.211-28A>G
NM_001302554.2:c.211-28A>G NP_001289483.1:n.211-28A>G
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