Canonical Allele Identifier: CA1748245414

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973668G= , CM000669.2:g.141973668G= GRCh38
NC_000007.13:g.141673468G= , CM000669.1:g.141673468G= GRCh37
NC_000007.12:g.141319937G= NCBI36
NG_016141.1:g.5106C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27671G= (MGAM) ENSP00000419372.1:n.-3+27671G=
ENST00000547270.1:c.22C= (TAS2R38) MANE Select ENSP00000448219.1:p.Arg8=
NM_176817.4:c.22C= (TAS2R38) NP_789787.4:p.Arg8=
XM_011515783.1:c.*25-12728G= (OR9A4) XP_011514085.1:n.*25-12728G=
NM_176817.5:c.22C= (TAS2R38) MANE Select NP_789787.5:p.Arg8=