Canonical Allele Identifier: CA355113586
Gene: BCHE HGNC NCBI

Linked Data

dbSNP Id: rs769875412

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.165830955G>C , CM000665.2:g.165830955G>C GRCh38
NC_000003.11:g.165548743G>C , CM000665.1:g.165548743G>C GRCh37
NC_000003.10:g.167031437G>C NCBI36
NG_009031.1:g.11511C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264381.8:c.79C>G MANE Select ENSP00000264381.3:p.His27Asp
ENST00000264381.7:c.79C>G ENSP00000264381.3:p.His27Asp
ENST00000479451.5:c.107+6359C>G ENSP00000418325.1:n.107+6359C>G
ENST00000482958.1:c.79C>G ENSP00000419804.1:p.His27Asp
ENST00000488954.1:c.107+6359C>G ENSP00000418504.1:n.107+6359C>G
ENST00000497011.5:c.79C>G ENSP00000419505.1:p.His27Asp
NM_000055.2:c.79C>G NP_000046.1:p.His27Asp
XM_005247685.1:c.202C>G XP_005247742.1:p.His68Asp
NM_000055.3:c.79C>G NP_000046.1:p.His27Asp
NR_137635.1:n.159+6359C>G
NR_137636.1:n.246C>G
NM_000055.4:c.79C>G MANE Select NP_000046.1:p.His27Asp
NR_137635.2:n.110+6359C>G
NR_137636.2:n.197C>G