Canonical Allele Identifier: CA1748243998

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141972640A= , CM000669.2:g.141972640A= GRCh38
NC_000007.13:g.141672440A= , CM000669.1:g.141672440A= GRCh37
NC_000007.12:g.141318909A= NCBI36
NG_016141.1:g.6134T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+26643A= (MGAM) ENSP00000419372.1:n.-3+26643A=
ENST00000547270.1:c.*48T= (TAS2R38) MANE Select ENSP00000448219.1:n.*48T=
NM_176817.4:c.*48T= (TAS2R38) NP_789787.4:n.*48T=
XM_011515783.1:c.*25-13756A= (OR9A4) XP_011514085.1:n.*25-13756A=
NM_176817.5:c.*48T= (TAS2R38) MANE Select NP_789787.5:n.*48T=