Canonical Allele Identifier: CA436818780

Gene: BCHE

Linked Data

• MyVariant Identifiers: chr3:g.165491293T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165773505T>A , CM000665.2:g.165773505T>A	GRCh38
NC_000003.11:g.165491293T>A , CM000665.1:g.165491293T>A	GRCh37
NC_000003.10:g.166973987T>A	NCBI36
NG_009031.1:g.68961A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000264381.8:c.1686A>T MANE Select	ENSP00000264381.3:p.Gly562=
ENST00000264381.7:c.1686A>T	ENSP00000264381.3:p.Gly562=
ENST00000479451.5:c.276A>T	ENSP00000418325.1:p.Gly92=
ENST00000482958.1:c.*192A>T	ENSP00000419804.1:n.*192A>T
ENST00000497011.5:c.*76A>T	ENSP00000419505.1:n.*76A>T
NM_000055.2:c.1686A>T	NP_000046.1:p.Gly562=
XM_005247685.1:c.1809A>T	XP_005247742.1:p.Gly603=
NM_000055.3:c.1686A>T	NP_000046.1:p.Gly562=
NR_137635.1:n.328A>T
NR_137636.1:n.1932A>T
NM_000055.4:c.1686A>T MANE Select	NP_000046.1:p.Gly562=
NR_137635.2:n.279A>T
NR_137636.2:n.1883A>T