Canonical Allele Identifier: CA87410379
Gene: BCHE HGNC NCBI

Linked Data

dbSNP Id: rs1044666393

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.165830861C>A , CM000665.2:g.165830861C>A GRCh38
NC_000003.11:g.165548649C>A , CM000665.1:g.165548649C>A GRCh37
NC_000003.10:g.167031343C>A NCBI36
NG_009031.1:g.11605G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264381.8:c.173G>T MANE Select ENSP00000264381.3:p.Gly58Val
ENST00000264381.7:c.173G>T ENSP00000264381.3:p.Gly58Val
ENST00000479451.5:c.107+6453G>T ENSP00000418325.1:n.107+6453G>T
ENST00000482958.1:c.173G>T ENSP00000419804.1:p.Gly58Val
ENST00000488954.1:c.107+6453G>T ENSP00000418504.1:n.107+6453G>T
ENST00000497011.5:c.173G>T ENSP00000419505.1:p.Gly58Val
NM_000055.2:c.173G>T NP_000046.1:p.Gly58Val
XM_005247685.1:c.296G>T XP_005247742.1:p.Gly99Val
NM_000055.3:c.173G>T NP_000046.1:p.Gly58Val
NR_137635.1:n.159+6453G>T
NR_137636.1:n.340G>T
NM_000055.4:c.173G>T MANE Select NP_000046.1:p.Gly58Val
NR_137635.2:n.110+6453G>T
NR_137636.2:n.291G>T