Canonical Allele Identifier: CA684419717
Gene: ACADS HGNC NCBI

Linked Data

dbSNP Id: rs1316691588
gnomAD v4: 12-120739709-G-T
MyVariant Identifiers: chr12:g.121177512G>T (hg19) chr12:g.120739709G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120739709G>T , CM000674.2:g.120739709G>T GRCh38
NC_000012.11:g.121177512G>T , CM000674.1:g.121177512G>T GRCh37
NC_000012.10:g.119661895G>T NCBI36
NG_007991.1:g.18942G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.*261G>T MANE Select ENSP00000242592.4:n.*261G>T
ENST00000242592.8:c.*261G>T ENSP00000242592.4:n.*261G>T
NM_000017.3:c.*261G>T NP_000008.1:n.*261G>T
NM_001302554.1:c.*261G>T NP_001289483.1:n.*261G>T
NM_000017.4:c.*261G>T MANE Select NP_000008.1:n.*261G>T
NM_001302554.2:c.*261G>T NP_001289483.1:n.*261G>T
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