Canonical Allele Identifier: CA436968890
Gene: BCHE HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.165547910T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.165830122T>C , CM000665.2:g.165830122T>C GRCh38
NC_000003.11:g.165547910T>C , CM000665.1:g.165547910T>C GRCh37
NC_000003.10:g.167030604T>C NCBI36
NG_009031.1:g.12344A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264381.8:c.912A>G MANE Select ENSP00000264381.3:p.Glu304=
ENST00000264381.7:c.912A>G ENSP00000264381.3:p.Glu304=
ENST00000479451.5:n.107+7192A>G ENSP00000418325.1:n.107+7192A>G
ENST00000482958.1:c.912A>G ENSP00000419804.1:p.Glu304=
ENST00000488954.1:n.107+7192A>G ENSP00000418504.1:n.107+7192A>G
ENST00000497011.5:c.912A>G ENSP00000419505.1:p.Glu304=
NM_000055.2:c.912A>G NP_000046.1:p.Glu304=
XM_005247685.1:c.1035A>G XP_005247742.1:p.Glu345=
NM_000055.3:c.912A>G NP_000046.1:p.Glu304=
NR_137635.1:n.159+7192A>G
NR_137636.1:n.1079A>G
NM_000055.4:c.912A>G MANE Select NP_000046.1:p.Glu304=
NR_137635.2:n.110+7192A>G
NR_137636.2:n.1030A>G