Canonical Allele Identifier: CA436968771

Gene: BCHE

Linked Data

• dbSNP Id: rs368885671
• gnomAD v2: 3-165547862-C-A
• gnomAD v4: 3-165830074-C-A
• MyVariant Identifiers: chr3:g.165547862C>A (hg19) ; chr3:g.165830074C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165830074C>A , CM000665.2:g.165830074C>A	GRCh38
NC_000003.11:g.165547862C>A , CM000665.1:g.165547862C>A	GRCh37
NC_000003.10:g.167030556C>A	NCBI36
NG_009031.1:g.12392G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264381.8:c.960G>T MANE Select	ENSP00000264381.3:p.Pro320=
ENST00000264381.7:c.960G>T	ENSP00000264381.3:p.Pro320=
ENST00000479451.5:c.107+7240G>T	ENSP00000418325.1:n.107+7240G>T
ENST00000482958.1:c.960G>T	ENSP00000419804.1:p.Pro320=
ENST00000488954.1:c.107+7240G>T	ENSP00000418504.1:n.107+7240G>T
ENST00000497011.5:c.960G>T	ENSP00000419505.1:p.Pro320=
NM_000055.2:c.960G>T	NP_000046.1:p.Pro320=
XM_005247685.1:c.1083G>T	XP_005247742.1:p.Pro361=
NM_000055.3:c.960G>T	NP_000046.1:p.Pro320=
NR_137635.1:n.159+7240G>T
NR_137636.1:n.1127G>T
NM_000055.4:c.960G>T MANE Select	NP_000046.1:p.Pro320=
NR_137635.2:n.110+7240G>T
NR_137636.2:n.1078G>T