Canonical Allele Identifier: CA87410333

Gene: BCHE

Linked Data

• dbSNP Id: rs945799475
• gnomAD v2: 3-165547933-G-A
• gnomAD v4: 3-165830145-G-A
• MyVariant Identifiers: chr3:g.165547933G>A (hg19) ; chr3:g.165830145G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165830145G>A , CM000665.2:g.165830145G>A	GRCh38
NC_000003.11:g.165547933G>A , CM000665.1:g.165547933G>A	GRCh37
NC_000003.10:g.167030627G>A	NCBI36
NG_009031.1:g.12321C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264381.8:c.889C>T MANE Select	ENSP00000264381.3:p.Pro297Ser
ENST00000264381.7:c.889C>T	ENSP00000264381.3:p.Pro297Ser
ENST00000479451.5:c.107+7169C>T	ENSP00000418325.1:n.107+7169C>T
ENST00000482958.1:c.889C>T	ENSP00000419804.1:p.Pro297Ser
ENST00000488954.1:c.107+7169C>T	ENSP00000418504.1:n.107+7169C>T
ENST00000497011.5:c.889C>T	ENSP00000419505.1:p.Pro297Ser
NM_000055.2:c.889C>T	NP_000046.1:p.Pro297Ser
XM_005247685.1:c.1012C>T	XP_005247742.1:p.Pro338Ser
NM_000055.3:c.889C>T	NP_000046.1:p.Pro297Ser
NR_137635.1:n.159+7169C>T
NR_137636.1:n.1056C>T
NM_000055.4:c.889C>T MANE Select	NP_000046.1:p.Pro297Ser
NR_137635.2:n.110+7169C>T
NR_137636.2:n.1007C>T