Canonical Allele Identifier: CA2692400
Gene: BCHE HGNC NCBI

Linked Data

dbSNP Id: rs368885671

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.165830074C>T , CM000665.2:g.165830074C>T GRCh38
NC_000003.11:g.165547862C>T , CM000665.1:g.165547862C>T GRCh37
NC_000003.10:g.167030556C>T NCBI36
NG_009031.1:g.12392G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264381.8:c.960G>A MANE Select ENSP00000264381.3:p.Pro320=
ENST00000264381.7:c.960G>A ENSP00000264381.3:p.Pro320=
ENST00000479451.5:c.107+7240G>A ENSP00000418325.1:n.107+7240G>A
ENST00000482958.1:c.960G>A ENSP00000419804.1:p.Pro320=
ENST00000488954.1:c.107+7240G>A ENSP00000418504.1:n.107+7240G>A
ENST00000497011.5:c.960G>A ENSP00000419505.1:p.Pro320=
NM_000055.2:c.960G>A NP_000046.1:p.Pro320=
XM_005247685.1:c.1083G>A XP_005247742.1:p.Pro361=
NM_000055.3:c.960G>A NP_000046.1:p.Pro320=
NR_137635.1:n.159+7240G>A
NR_137636.1:n.1127G>A
NM_000055.4:c.960G>A MANE Select NP_000046.1:p.Pro320=
NR_137635.2:n.110+7240G>A
NR_137636.2:n.1078G>A