Canonical Allele Identifier: CA436969120

Gene: BCHE

Linked Data

• MyVariant Identifiers: chr3:g.165548020T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165830232T>G , CM000665.2:g.165830232T>G	GRCh38
NC_000003.11:g.165548020T>G , CM000665.1:g.165548020T>G	GRCh37
NC_000003.10:g.167030714T>G	NCBI36
NG_009031.1:g.12234A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000264381.8:c.802A>C MANE Select	ENSP00000264381.3:p.Arg268=
ENST00000264381.7:c.802A>C	ENSP00000264381.3:p.Arg268=
ENST00000479451.5:c.107+7082A>C	ENSP00000418325.1:n.107+7082A>C
ENST00000482958.1:c.802A>C	ENSP00000419804.1:p.Arg268=
ENST00000488954.1:c.107+7082A>C	ENSP00000418504.1:n.107+7082A>C
ENST00000497011.5:c.802A>C	ENSP00000419505.1:p.Arg268=
NM_000055.2:c.802A>C	NP_000046.1:p.Arg268=
XM_005247685.1:c.925A>C	XP_005247742.1:p.Arg309=
NM_000055.3:c.802A>C	NP_000046.1:p.Arg268=
NR_137635.1:n.159+7082A>C
NR_137636.1:n.969A>C
NM_000055.4:c.802A>C MANE Select	NP_000046.1:p.Arg268=
NR_137635.2:n.110+7082A>C
NR_137636.2:n.920A>C