Canonical Allele Identifier: CA2067556016
Gene: ACADS HGNC NCBI

Linked Data

dbSNP Id: rs1883597517

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120739707G>T , CM000674.2:g.120739707G>T GRCh38
NC_000012.11:g.121177510G>T , CM000674.1:g.121177510G>T GRCh37
NC_000012.10:g.119661893G>T NCBI36
NG_007991.1:g.18940G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.*259G>T MANE Select ENSP00000242592.4:n.*259G>T
ENST00000242592.8:c.*259G>T ENSP00000242592.4:n.*259G>T
NM_000017.3:c.*259G>T NP_000008.1:n.*259G>T
NM_001302554.1:c.*259G>T NP_001289483.1:n.*259G>T
NM_000017.4:c.*259G>T MANE Select NP_000008.1:n.*259G>T
NM_001302554.2:c.*259G>T NP_001289483.1:n.*259G>T