Canonical Allele Identifier: CA1417711999

Gene: BCHE

Linked Data

• dbSNP Id: rs1712957016

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165786481A>G , CM000665.2:g.165786481A>G	GRCh38
NC_000003.11:g.165504269A>G , CM000665.1:g.165504269A>G	GRCh37
NC_000003.10:g.166986963A>G	NCBI36
NG_009031.1:g.55985T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264381.8:c.1518-170T>C MANE Select	ENSP00000264381.3:n.1518-170T>C
ENST00000264381.7:c.1518-170T>C	ENSP00000264381.3:n.1518-170T>C
ENST00000479451.5:c.108-170T>C	ENSP00000418325.1:n.108-170T>C
ENST00000482958.1:c.*24-170T>C	ENSP00000419804.1:n.*24-170T>C
ENST00000488954.1:c.108-170T>C	ENSP00000418504.1:n.108-170T>C
ENST00000497011.5:c.1518-170T>C	ENSP00000419505.1:n.1518-170T>C
NM_000055.2:c.1518-170T>C	NP_000046.1:n.1518-170T>C
XM_005247685.1:c.1641-170T>C	XP_005247742.1:n.1641-170T>C
NM_000055.3:c.1518-170T>C	NP_000046.1:n.1518-170T>C
NR_137635.1:n.160-170T>C
NR_137636.1:n.1685-170T>C
NM_000055.4:c.1518-170T>C MANE Select	NP_000046.1:n.1518-170T>C
NR_137635.2:n.111-170T>C
NR_137636.2:n.1636-170T>C