Canonical Allele Identifier: CA1748244215

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141972786C= , CM000669.2:g.141972786C= GRCh38
NC_000007.13:g.141672586C= , CM000669.1:g.141672586C= GRCh37
NC_000007.12:g.141319055C= NCBI36
NG_016141.1:g.5988G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+26789C= (MGAM) ENSP00000419372.1:n.-3+26789C=
ENST00000547270.1:c.904G= (TAS2R38) MANE Select ENSP00000448219.1:p.Ala302=
NM_176817.4:c.904G= (TAS2R38) NP_789787.4:p.Ala302=
XM_011515783.1:c.*25-13610C= (OR9A4) XP_011514085.1:n.*25-13610C=
NM_176817.5:c.904G= (TAS2R38) MANE Select NP_789787.5:p.Ala302=