Canonical Allele Identifier: CA355112744

Gene: BCHE

Linked Data

• dbSNP Id: rs121918558
• gnomAD v2: 3-165548355-T-G
• gnomAD v3: 3-165830567-T-G
• gnomAD v4: 3-165830567-T-G
• MyVariant Identifiers: chr3:g.165548355T>G (hg19) ; chr3:g.165830567T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165830567T>G , CM000665.2:g.165830567T>G	GRCh38
NC_000003.11:g.165548355T>G , CM000665.1:g.165548355T>G	GRCh37
NC_000003.10:g.167031049T>G	NCBI36
NG_009031.1:g.11899A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000264381.8:c.467A>C MANE Select	ENSP00000264381.3:p.Tyr156Ser
ENST00000264381.7:c.467A>C	ENSP00000264381.3:p.Tyr156Ser
ENST00000479451.5:c.107+6747A>C	ENSP00000418325.1:n.107+6747A>C
ENST00000482958.1:c.467A>C	ENSP00000419804.1:p.Tyr156Ser
ENST00000488954.1:c.107+6747A>C	ENSP00000418504.1:n.107+6747A>C
ENST00000497011.5:c.467A>C	ENSP00000419505.1:p.Tyr156Ser
NM_000055.2:c.467A>C	NP_000046.1:p.Tyr156Ser
XM_005247685.1:c.590A>C	XP_005247742.1:p.Tyr197Ser
NM_000055.3:c.467A>C	NP_000046.1:p.Tyr156Ser
NR_137635.1:n.159+6747A>C
NR_137636.1:n.634A>C
NM_000055.4:c.467A>C MANE Select	NP_000046.1:p.Tyr156Ser
NR_137635.2:n.110+6747A>C
NR_137636.2:n.585A>C