Canonical Allele Identifier: CA355111754

Gene: BCHE

Linked Data

• dbSNP Id: rs572660949
• gnomAD v3: 3-165830097-G-C
• gnomAD v4: 3-165830097-G-C
• MyVariant Identifiers: chr3:g.165547885G>C (hg19) ; chr3:g.165830097G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165830097G>C , CM000665.2:g.165830097G>C	GRCh38
NC_000003.11:g.165547885G>C , CM000665.1:g.165547885G>C	GRCh37
NC_000003.10:g.167030579G>C	NCBI36
NG_009031.1:g.12369C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264381.8:c.937C>G MANE Select	ENSP00000264381.3:p.Pro313Ala
ENST00000264381.7:c.937C>G	ENSP00000264381.3:p.Pro313Ala
ENST00000479451.5:c.107+7217C>G	ENSP00000418325.1:n.107+7217C>G
ENST00000482958.1:c.937C>G	ENSP00000419804.1:p.Pro313Ala
ENST00000488954.1:c.107+7217C>G	ENSP00000418504.1:n.107+7217C>G
ENST00000497011.5:c.937C>G	ENSP00000419505.1:p.Pro313Ala
NM_000055.2:c.937C>G	NP_000046.1:p.Pro313Ala
XM_005247685.1:c.1060C>G	XP_005247742.1:p.Pro354Ala
NM_000055.3:c.937C>G	NP_000046.1:p.Pro313Ala
NR_137635.1:n.159+7217C>G
NR_137636.1:n.1104C>G
NM_000055.4:c.937C>G MANE Select	NP_000046.1:p.Pro313Ala
NR_137635.2:n.110+7217C>G
NR_137636.2:n.1055C>G