Canonical Allele Identifier: CA436969116

Gene: BCHE

Linked Data

• dbSNP Id: rs1205357464
• gnomAD v2: 3-165548288-G-A
• gnomAD v4: 3-165830500-G-A
• MyVariant Identifiers: chr3:g.165548288G>A (hg19) ; chr3:g.165830500G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165830500G>A , CM000665.2:g.165830500G>A	GRCh38
NC_000003.11:g.165548288G>A , CM000665.1:g.165548288G>A	GRCh37
NC_000003.10:g.167030982G>A	NCBI36
NG_009031.1:g.11966C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000264381.8:c.534C>T MANE Select	ENSP00000264381.3:p.Ala178=
ENST00000264381.7:c.534C>T	ENSP00000264381.3:p.Ala178=
ENST00000479451.5:c.107+6814C>T	ENSP00000418325.1:n.107+6814C>T
ENST00000482958.1:c.534C>T	ENSP00000419804.1:p.Ala178=
ENST00000488954.1:c.107+6814C>T	ENSP00000418504.1:n.107+6814C>T
ENST00000497011.5:c.534C>T	ENSP00000419505.1:p.Ala178=
NM_000055.2:c.534C>T	NP_000046.1:p.Ala178=
XM_005247685.1:c.657C>T	XP_005247742.1:p.Ala219=
NM_000055.3:c.534C>T	NP_000046.1:p.Ala178=
NR_137635.1:n.159+6814C>T
NR_137636.1:n.701C>T
NM_000055.4:c.534C>T MANE Select	NP_000046.1:p.Ala178=
NR_137635.2:n.110+6814C>T
NR_137636.2:n.652C>T