Canonical Allele Identifier: CA87406613
Gene: BCHE HGNC NCBI

Linked Data

dbSNP Id: rs779039120

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.165798716G>A , CM000665.2:g.165798716G>A GRCh38
NC_000003.11:g.165516504G>A , CM000665.1:g.165516504G>A GRCh37
NC_000003.10:g.166999198G>A NCBI36
NG_009031.1:g.43750C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264381.8:c.1518-12405C>T MANE Select ENSP00000264381.3:n.1518-12405C>T
ENST00000264381.7:c.1518-12405C>T ENSP00000264381.3:n.1518-12405C>T
ENST00000479451.5:c.108-12405C>T ENSP00000418325.1:n.108-12405C>T
ENST00000482958.1:c.*24-12405C>T ENSP00000419804.1:n.*24-12405C>T
ENST00000488954.1:c.108-12405C>T ENSP00000418504.1:n.108-12405C>T
ENST00000497011.5:c.1518-12405C>T ENSP00000419505.1:n.1518-12405C>T
NM_000055.2:c.1518-12405C>T NP_000046.1:n.1518-12405C>T
XM_005247685.1:c.1641-12405C>T XP_005247742.1:n.1641-12405C>T
NM_000055.3:c.1518-12405C>T NP_000046.1:n.1518-12405C>T
NR_137635.1:n.160-12405C>T
NR_137636.1:n.1685-12405C>T
NM_000055.4:c.1518-12405C>T MANE Select NP_000046.1:n.1518-12405C>T
NR_137635.2:n.111-12405C>T
NR_137636.2:n.1636-12405C>T