Canonical Allele Identifier: CA2692582
Gene: BCHE HGNC NCBI

Linked Data

dbSNP Id: rs149985624

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.165831025G>T , CM000665.2:g.165831025G>T GRCh38
NC_000003.11:g.165548813G>T , CM000665.1:g.165548813G>T GRCh37
NC_000003.10:g.167031507G>T NCBI36
NG_009031.1:g.11441C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264381.8:c.9C>A MANE Select ENSP00000264381.3:p.Ser3Arg
ENST00000264381.7:c.9C>A ENSP00000264381.3:p.Ser3Arg
ENST00000479451.5:c.107+6289C>A ENSP00000418325.1:n.107+6289C>A
ENST00000482958.1:c.9C>A ENSP00000419804.1:p.Ser3Arg
ENST00000488954.1:c.107+6289C>A ENSP00000418504.1:n.107+6289C>A
ENST00000497011.5:c.9C>A ENSP00000419505.1:p.Ser3Arg
NM_000055.2:c.9C>A NP_000046.1:p.Ser3Arg
XM_005247685.1:c.132C>A XP_005247742.1:p.Ser44Arg
NM_000055.3:c.9C>A NP_000046.1:p.Ser3Arg
NR_137635.1:n.159+6289C>A
NR_137636.1:n.176C>A
NM_000055.4:c.9C>A MANE Select NP_000046.1:p.Ser3Arg
NR_137635.2:n.110+6289C>A
NR_137636.2:n.127C>A