Canonical Allele Identifier: CA16040923
Gene: BCHE HGNC NCBI

Linked Data

ClinVar Variation Id: 371431
ClinVar RCV Id: RCV000412007
dbSNP Id: rs1057517265
MyVariant Identifiers: chr3:g.165547807G>A (hg19) chr3:g.165830019G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.165830019G>A , CM000665.2:g.165830019G>A GRCh38
NC_000003.11:g.165547807G>A , CM000665.1:g.165547807G>A GRCh37
NC_000003.10:g.167030501G>A NCBI36
NG_009031.1:g.12447C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264381.8:c.1015C>T MANE Select ENSP00000264381.3:p.Gln339Ter
ENST00000264381.7:c.1015C>T ENSP00000264381.3:p.Gln339Ter
ENST00000479451.5:c.107+7295C>T ENSP00000418325.1:n.107+7295C>T
ENST00000482958.1:c.1015C>T ENSP00000419804.1:p.Gln339Ter
ENST00000488954.1:c.107+7295C>T ENSP00000418504.1:n.107+7295C>T
ENST00000497011.5:c.1015C>T ENSP00000419505.1:p.Gln339Ter
NM_000055.2:c.1015C>T NP_000046.1:p.Gln339Ter
XM_005247685.1:c.1138C>T XP_005247742.1:p.Gln380Ter
NM_000055.3:c.1015C>T NP_000046.1:p.Gln339Ter
NR_137635.1:n.159+7295C>T
NR_137636.1:n.1182C>T
NM_000055.4:c.1015C>T MANE Select NP_000046.1:p.Gln339Ter
NR_137635.2:n.110+7295C>T
NR_137636.2:n.1133C>T
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