Allele Registry

Canonical Allele Identifier: CA10869360

Gene: TAS1R3 HGNC NCBI

Linked Data - Predicted Effect Evidence

MyVariant.info:

GRCh38 chr1:g.1330080T>C

GRCh37 chr1:g.1265460T>C

Linked Data - Sequence & Population

gnomAD v2:

1:1265460 T / C

gnomAD v3:

1:1330080 T / C

gnomAD v4:

chr1-1330080-T-C

Joint Max Group AF 0.9274258 (NFE)

Genomes Max Group AF 0.9274258 (NFE)

Linked Data - NCBI & NCI

dbSNP:

35744813

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1330080T>C , CM000663.2:g.1330080T>C	GRCh38
NC_000001.10:g.1265460T>C , CM000663.1:g.1265460T>C	GRCh37
NC_000001.9:g.1255323T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011542239.1:c.-1266T>C	XP_011540541.1:n.-1266T>C

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