Canonical Allele Identifier: CA902030098

Gene: BCHE

Linked Data

• dbSNP Id: rs1800581
• MyVariant Identifiers: chr3:g.165548837A>G (hg19) ; chr3:g.165831049A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165831049A>G , CM000665.2:g.165831049A>G	GRCh38
NC_000003.11:g.165548837A>G , CM000665.1:g.165548837A>G	GRCh37
NC_000003.10:g.167031531A>G	NCBI36
NG_009031.1:g.11417T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264381.8:c.-8-8T>C MANE Select	ENSP00000264381.3:n.-8-8T>C
ENST00000264381.7:c.-8-8T>C	ENSP00000264381.3:n.-8-8T>C
ENST00000479451.5:c.107+6265T>C	ENSP00000418325.1:n.107+6265T>C
ENST00000482958.1:c.-8-8T>C	ENSP00000419804.1:n.-8-8T>C
ENST00000488954.1:c.107+6265T>C	ENSP00000418504.1:n.107+6265T>C
ENST00000497011.5:c.-8-8T>C	ENSP00000419505.1:n.-8-8T>C
NM_000055.2:c.-8-8T>C	NP_000046.1:n.-8-8T>C
XM_005247685.1:c.116-8T>C	XP_005247742.1:n.116-8T>C
NM_000055.3:c.-8-8T>C	NP_000046.1:n.-8-8T>C
NR_137635.1:n.159+6265T>C
NR_137636.1:n.160-8T>C
NM_000055.4:c.-8-8T>C MANE Select	NP_000046.1:n.-8-8T>C
NR_137635.2:n.110+6265T>C
NR_137636.2:n.111-8T>C