Canonical Allele Identifier: CA436818779

Gene: BCHE

Linked Data

• MyVariant Identifiers: chr3:g.165491290A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165773502A>G , CM000665.2:g.165773502A>G	GRCh38
NC_000003.11:g.165491290A>G , CM000665.1:g.165491290A>G	GRCh37
NC_000003.10:g.166973984A>G	NCBI36
NG_009031.1:g.68964T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000264381.8:c.1689T>C MANE Select	ENSP00000264381.3:p.Asn563=
ENST00000264381.7:c.1689T>C	ENSP00000264381.3:p.Asn563=
ENST00000479451.5:c.279T>C	ENSP00000418325.1:p.Asn93=
ENST00000482958.1:c.*195T>C	ENSP00000419804.1:n.*195T>C
ENST00000497011.5:c.*79T>C	ENSP00000419505.1:n.*79T>C
NM_000055.2:c.1689T>C	NP_000046.1:p.Asn563=
XM_005247685.1:c.1812T>C	XP_005247742.1:p.Asn604=
NM_000055.3:c.1689T>C	NP_000046.1:p.Asn563=
NR_137635.1:n.331T>C
NR_137636.1:n.1935T>C
NM_000055.4:c.1689T>C MANE Select	NP_000046.1:p.Asn563=
NR_137635.2:n.282T>C
NR_137636.2:n.1886T>C