Canonical Allele Identifier: CA87410352

Gene: BCHE

Linked Data

• dbSNP Id: rs151020233
• gnomAD v2: 3-165548261-A-T
• gnomAD v3: 3-165830473-A-T
• gnomAD v4: 3-165830473-A-T
• MyVariant Identifiers: chr3:g.165548261A>T (hg19) ; chr3:g.165830473A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165830473A>T , CM000665.2:g.165830473A>T	GRCh38
NC_000003.11:g.165548261A>T , CM000665.1:g.165548261A>T	GRCh37
NC_000003.10:g.167030955A>T	NCBI36
NG_009031.1:g.11993T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000264381.8:c.561T>A MANE Select	ENSP00000264381.3:p.Asn187Lys
ENST00000264381.7:c.561T>A	ENSP00000264381.3:p.Asn187Lys
ENST00000479451.5:c.107+6841T>A	ENSP00000418325.1:n.107+6841T>A
ENST00000482958.1:c.561T>A	ENSP00000419804.1:p.Asn187Lys
ENST00000488954.1:c.107+6841T>A	ENSP00000418504.1:n.107+6841T>A
ENST00000497011.5:c.561T>A	ENSP00000419505.1:p.Asn187Lys
NM_000055.2:c.561T>A	NP_000046.1:p.Asn187Lys
XM_005247685.1:c.684T>A	XP_005247742.1:p.Asn228Lys
NM_000055.3:c.561T>A	NP_000046.1:p.Asn187Lys
NR_137635.1:n.159+6841T>A
NR_137636.1:n.728T>A
NM_000055.4:c.561T>A MANE Select	NP_000046.1:p.Asn187Lys
NR_137635.2:n.110+6841T>A
NR_137636.2:n.679T>A