Canonical Allele Identifier: CA2067555492
Gene: ACADS HGNC NCBI

Linked Data

dbSNP Id: rs1883547750

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120738766C>T , CM000674.2:g.120738766C>T GRCh38
NC_000012.11:g.121176569C>T , CM000674.1:g.121176569C>T GRCh37
NC_000012.10:g.119660952C>T NCBI36
NG_007991.1:g.17999C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000242592.9:c.934-54C>T MANE Select ENSP00000242592.4:n.934-54C>T
ENST00000242592.8:c.934-54C>T ENSP00000242592.4:n.934-54C>T
ENST00000411593.2:c.922-54C>T ENSP00000401045.2:n.922-54C>T
NM_000017.3:c.934-54C>T NP_000008.1:n.934-54C>T
NM_001302554.1:c.922-54C>T NP_001289483.1:n.922-54C>T
NM_000017.4:c.934-54C>T MANE Select NP_000008.1:n.934-54C>T
NM_001302554.2:c.922-54C>T NP_001289483.1:n.922-54C>T