Canonical Allele Identifier: CA1748245174

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973454G= , CM000669.2:g.141973454G= GRCh38
NC_000007.13:g.141673254G= , CM000669.1:g.141673254G= GRCh37
NC_000007.12:g.141319723G= NCBI36
NG_016141.1:g.5320C=

Transcript Alleles

HGVS Amino-acid change
ENST00000465654.5:c.-3+27457G= (MGAM) ENSP00000419372.1:n.-3+27457G=
ENST00000547270.1:c.236C= (TAS2R38) MANE Select ENSP00000448219.1:p.Thr79=
NM_176817.4:c.236C= (TAS2R38) NP_789787.4:p.Thr79=
XM_011515783.1:c.*25-12942G= (OR9A4) XP_011514085.1:n.*25-12942G=
NM_176817.5:c.236C= (TAS2R38) MANE Select NP_789787.5:p.Thr79=