Canonical Allele Identifier: CA458161934
Gene: TAS2R38 HGNC NCBI
OR9A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.141673253G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973453G>T , CM000669.2:g.141973453G>T GRCh38
NC_000007.13:g.141673253G>T , CM000669.1:g.141673253G>T GRCh37
NC_000007.12:g.141319722G>T NCBI36
NG_016141.1:g.5321C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000465654.5:c.-3+27456G>T ENSP00000419372.1:p.=
ENST00000547270.1:c.237C>A MANE Select ENSP00000448219.1:p.Thr79=
NM_176817.4:c.237C>A (TAS2R38) NP_789787.4:p.Thr79=
XM_011515783.1:c.*25-12943G>T (OR9A4) XP_011514085.1:p.=
NM_176817.5:c.237C>A (TAS2R38) MANE Select NP_789787.5:p.Thr79=