Canonical Allele Identifier: CA2727324390
Gene: ACADS HGNC NCBI

Linked Data

dbSNP Id: rs2136951501

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120739646T>G , CM000674.2:g.120739646T>G GRCh38
NC_000012.11:g.121177449T>G , CM000674.1:g.121177449T>G GRCh37
NC_000012.10:g.119661832T>G NCBI36
NG_007991.1:g.18879T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.*198T>G MANE Select ENSP00000242592.4:n.*198T>G
ENST00000242592.8:c.*198T>G ENSP00000242592.4:n.*198T>G
NM_000017.3:c.*198T>G NP_000008.1:n.*198T>G
NM_001302554.1:c.*198T>G NP_001289483.1:n.*198T>G
NM_000017.4:c.*198T>G MANE Select NP_000008.1:n.*198T>G
NM_001302554.2:c.*198T>G NP_001289483.1:n.*198T>G