Canonical Allele Identifier: CA2611279631

Gene: ACADSB

Linked Data

• gnomAD v4: 10-123052938-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.123052938G>T , CM000672.2:g.123052938G>T	GRCh38
NC_000010.10:g.124812454G>T , CM000672.1:g.124812454G>T	GRCh37
NC_000010.9:g.124802444G>T	NCBI36
NG_008003.1:g.49026G>T , LRG_451:g.49026G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000358776.7:c.1129-123G>T MANE Select	ENSP00000357873.3:n.1129-123G>T
ENST00000358776.6:c.1129-123G>T	ENSP00000357873.3:n.1129-123G>T
ENST00000368869.8:c.823-123G>T	ENSP00000357862.4:n.823-123G>T
ENST00000541070.1:n.178G>T
NM_001609.3:c.1129-123G>T , LRG_451t1:c.1129-123G>T	NP_001600.1:n.1129-123G>T
NM_001330174.1:c.823-123G>T	NP_001317103.1:n.823-123G>T
NM_001330174.2:c.823-123G>T	NP_001317103.1:n.823-123G>T
NM_001609.4:c.1129-123G>T MANE Select	NP_001600.1:n.1129-123G>T
NM_001330174.3:c.823-123G>T	NP_001317103.1:n.823-123G>T