Canonical Allele Identifier: CA520605126
Gene: TAS1R3 HGNC NCBI

Linked Data

dbSNP Id: rs147788788
gnomAD v2: 1-1265572-C-A
gnomAD v3: 1-1330192-C-A
gnomAD v4: 1-1330192-C-A
MyVariant Identifiers: chr1:g.1265572_1265576delinsAGTTT (hg19) chr1:g.1330192_1330196delinsAGTTT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1330192C>A , CM000663.2:g.1330192C>A GRCh38
NC_000001.10:g.1265572C>A , CM000663.1:g.1265572C>A GRCh37
NC_000001.9:g.1255435C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011542239.1:c.-1154C>A XP_011540541.1:n.-1154C>A
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