Allele Registry

Canonical Allele Identifier: CA228696434

Gene: HTR3B HGNC NCBI

Linked Data - Predicted Effect Evidence

MyVariant.info:

GRCh38 chr11:g.113904553T>C

GRCh37 chr11:g.113775275T>C

Linked Data - Sequence & Population

gnomAD v2:

11:113775275 T / C

gnomAD v3:

11:113904553 T / C

gnomAD v4:

chr11-113904553-T-C

Joint Max Group AF 0.36635454 (AFR)

Genomes Max Group AF 0.36676538 (AFR)

Exomes Max Group AF 0.30315788 (AFR)

Linked Data - NCBI & NCI

dbSNP:

3758987

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113904553T>C , CM000673.2:g.113904553T>C	GRCh38
NC_000011.9:g.113775275T>C , CM000673.1:g.113775275T>C	GRCh37
NC_000011.8:g.113280485T>C	NCBI36
NG_011483.1:g.4687T>C

Transcript Alleles

HGVS	Amino-acid Change
XM_011543064.1:c.12+5470T>C	XP_011541366.1:n.12+5470T>C
XM_024448767.1:c.-242-4742T>C	XP_024304535.1:n.-242-4742T>C

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