Canonical Allele Identifier: CA2692422

Gene: BCHE

Linked Data

• dbSNP Id: rs779456773
• ExAC: 3:165547997 A / C
• gnomAD v2: 3-165547997-A-C
• gnomAD v4: 3-165830209-A-C
• MyVariant Identifiers: chr3:g.165547997A>C (hg19) ; chr3:g.165830209A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165830209A>C , CM000665.2:g.165830209A>C	GRCh38
NC_000003.11:g.165547997A>C , CM000665.1:g.165547997A>C	GRCh37
NC_000003.10:g.167030691A>C	NCBI36
NG_009031.1:g.12257T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264381.8:c.825T>G MANE Select	ENSP00000264381.3:p.Ala275=
ENST00000264381.7:c.825T>G	ENSP00000264381.3:p.Ala275=
ENST00000479451.5:c.107+7105T>G	ENSP00000418325.1:n.107+7105T>G
ENST00000482958.1:c.825T>G	ENSP00000419804.1:p.Ala275=
ENST00000488954.1:c.107+7105T>G	ENSP00000418504.1:n.107+7105T>G
ENST00000497011.5:c.825T>G	ENSP00000419505.1:p.Ala275=
NM_000055.2:c.825T>G	NP_000046.1:p.Ala275=
XM_005247685.1:c.948T>G	XP_005247742.1:p.Ala316=
NM_000055.3:c.825T>G	NP_000046.1:p.Ala275=
NR_137635.1:n.159+7105T>G
NR_137636.1:n.992T>G
NM_000055.4:c.825T>G MANE Select	NP_000046.1:p.Ala275=
NR_137635.2:n.110+7105T>G
NR_137636.2:n.943T>G