Canonical Allele Identifier: CA369564766

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973187A>T , CM000669.2:g.141973187A>T GRCh38
NC_000007.13:g.141672987A>T , CM000669.1:g.141672987A>T GRCh37
NC_000007.12:g.141319456A>T NCBI36
NG_016141.1:g.5587T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27190A>T (MGAM) ENSP00000419372.1:n.-3+27190A>T
ENST00000547270.1:c.503T>A (TAS2R38) MANE Select ENSP00000448219.1:p.Phe168Tyr
NM_176817.4:c.503T>A (TAS2R38) NP_789787.4:p.Phe168Tyr
XM_011515783.1:c.*25-13209A>T (OR9A4) XP_011514085.1:n.*25-13209A>T
NM_176817.5:c.503T>A (TAS2R38) MANE Select NP_789787.5:p.Phe168Tyr