Canonical Allele Identifier: CA369565662

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973452G>A , CM000669.2:g.141973452G>A GRCh38
NC_000007.13:g.141673252G>A , CM000669.1:g.141673252G>A GRCh37
NC_000007.12:g.141319721G>A NCBI36
NG_016141.1:g.5322C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000465654.5:c.-3+27455G>A (MGAM) ENSP00000419372.1:n.-3+27455G>A
ENST00000547270.1:c.238C>T (TAS2R38) MANE Select ENSP00000448219.1:p.His80Tyr
NM_176817.4:c.238C>T (TAS2R38) NP_789787.4:p.His80Tyr
XM_011515783.1:c.*25-12944G>A (OR9A4) XP_011514085.1:n.*25-12944G>A
NM_176817.5:c.238C>T (TAS2R38) MANE Select NP_789787.5:p.His80Tyr