Canonical Allele Identifier: CA355113558
Gene: BCHE HGNC NCBI

Linked Data

dbSNP Id: rs1418971053

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.165830943C>T , CM000665.2:g.165830943C>T GRCh38
NC_000003.11:g.165548731C>T , CM000665.1:g.165548731C>T GRCh37
NC_000003.10:g.167031425C>T NCBI36
NG_009031.1:g.11523G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264381.8:c.91G>A MANE Select ENSP00000264381.3:p.Asp31Asn
ENST00000264381.7:c.91G>A ENSP00000264381.3:p.Asp31Asn
ENST00000479451.5:c.107+6371G>A ENSP00000418325.1:n.107+6371G>A
ENST00000482958.1:c.91G>A ENSP00000419804.1:p.Asp31Asn
ENST00000488954.1:c.107+6371G>A ENSP00000418504.1:n.107+6371G>A
ENST00000497011.5:c.91G>A ENSP00000419505.1:p.Asp31Asn
NM_000055.2:c.91G>A NP_000046.1:p.Asp31Asn
XM_005247685.1:c.214G>A XP_005247742.1:p.Asp72Asn
NM_000055.3:c.91G>A NP_000046.1:p.Asp31Asn
NR_137635.1:n.159+6371G>A
NR_137636.1:n.258G>A
NM_000055.4:c.91G>A MANE Select NP_000046.1:p.Asp31Asn
NR_137635.2:n.110+6371G>A
NR_137636.2:n.209G>A