Canonical Allele Identifier: CA10770732

Gene: ACOT11

Linked Data

• dbSNP Id: rs12411181
• gnomAD v2: 1-55091552-C-T
• gnomAD v3: 1-54625879-C-T
• gnomAD v4: 1-54625879-C-T
• MyVariant Identifiers: chr1:g.55091552C>T (hg19) ; chr1:g.54625879C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54625879C>T , CM000663.2:g.54625879C>T	GRCh38
NC_000001.10:g.55091552C>T , CM000663.1:g.55091552C>T	GRCh37
NC_000001.9:g.54864140C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371316.3:c.1630-4855C>T	ENSP00000360366.3:n.1630-4855C>T
NM_015547.3:c.1630-4855C>T	NP_056362.1:n.1630-4855C>T
NM_015547.4:c.1630-4855C>T	NP_056362.1:n.1630-4855C>T