Canonical Allele Identifier: CA519598
Gene: TAS1R3 HGNC NCBI

Linked Data

dbSNP Id: rs307377
gnomAD v2: 1-1269554-T-A
gnomAD v4: 1-1334174-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1334174T>A , CM000663.2:g.1334174T>A GRCh38
NC_000001.10:g.1269554T>A , CM000663.1:g.1269554T>A GRCh37
NC_000001.9:g.1259417T>A NCBI36
NG_008048.1:g.19939A>T
NG_008048.2:g.19939A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000339381.6:c.2269T>A MANE Select ENSP00000344411.5:p.Cys757Ser
ENST00000339381.5:c.2269T>A ENSP00000344411.5:p.Cys757Ser
XM_011542239.1:c.2266T>A XP_011540541.1:p.Cys756Ser
XM_017002435.1:c.2395T>A XP_016857924.1:p.Cys799Ser
XM_017002436.1:c.2392T>A XP_016857925.1:p.Cys798Ser
NM_152228.3:c.2269T>A MANE Select NP_689414.2:p.Cys757Ser