Canonical Allele Identifier: CA369565669
Gene: TAS2R38 HGNC NCBI
OR9A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973455T>A , CM000669.2:g.141973455T>A GRCh38
NC_000007.13:g.141673255T>A , CM000669.1:g.141673255T>A GRCh37
NC_000007.12:g.141319724T>A NCBI36
NG_016141.1:g.5319A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000465654.5:c.-3+27458T>A ENSP00000419372.1:p.=
ENST00000547270.1:c.235A>T MANE Select ENSP00000448219.1:p.Thr79Ser
NM_176817.4:c.235A>T (TAS2R38) NP_789787.4:p.Thr79Ser
XM_011515783.1:c.*25-12941T>A (OR9A4) XP_011514085.1:p.=
NM_176817.5:c.235A>T (TAS2R38) MANE Select NP_789787.5:p.Thr79Ser