Canonical Allele Identifier: CA15123653
Gene: TAS1R1 HGNC NCBI
MyVariant.info:
GRCh38 chr1:g.6571371C>T
GRCh37 chr1:g.6631431C>T
gnomAD v2:
1:6631431 C / T
gnomAD v3:
1:6571371 C / T
gnomAD v4:
chr1-6571371-C-T
Joint Max Group AF 0.86349978 (NFE)
Genomes Max Group AF 0.86349978 (NFE)
dbSNP:
11587438
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.6571371C>T , CM000663.2:g.6571371C>T GRCh38
NC_000001.10:g.6631431C>T , CM000663.1:g.6631431C>T GRCh37
NC_000001.9:g.6554018C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000333172.11:c.498+156C>T MANE Select ENSP00000331867.6:n.498+156C>T
ENST00000328191.5:c.264+156C>T ENSP00000327705.5:n.264+156C>T
ENST00000333172.10:c.498+156C>T ENSP00000331867.6:n.498+156C>T
ENST00000351136.7:c.498+156C>T ENSP00000312558.5:n.498+156C>T
ENST00000411823.5:c.275+156C>T
ENST00000415267.1:c.275+156C>T
NM_138697.3:c.498+156C>T NP_619642.2:n.498+156C>T
NM_177540.2:c.498+156C>T NP_803884.1:n.498+156C>T
XM_011542202.1:c.384+156C>T XP_011540504.1:n.384+156C>T
XM_011542203.1:c.264+156C>T XP_011540505.1:n.264+156C>T
XM_011542204.1:c.264+156C>T XP_011540506.1:n.264+156C>T
XM_011542206.1:c.504+156C>T XP_011540508.1:n.504+156C>T
XM_011542203.2:c.264+156C>T XP_011540505.1:n.264+156C>T
XM_011542206.2:c.504+156C>T XP_011540508.1:n.504+156C>T
XM_017002402.1:c.504+156C>T XP_016857891.1:n.504+156C>T
XM_017002403.1:c.504+156C>T XP_016857892.1:n.504+156C>T
XR_001737881.1:n.88-1388G>A
XR_002958250.1:n.88-1388G>A
NM_138697.4:c.498+156C>T MANE Select NP_619642.2:n.498+156C>T
NM_177540.3:c.498+156C>T NP_803884.1:n.498+156C>T
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