Canonical Allele Identifier: CA1748245158

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973446G= , CM000669.2:g.141973446G= GRCh38
NC_000007.13:g.141673246G= , CM000669.1:g.141673246G= GRCh37
NC_000007.12:g.141319715G= NCBI36
NG_016141.1:g.5328C=

Transcript Alleles

HGVS Amino-acid change
ENST00000465654.5:c.-3+27449G= (MGAM) ENSP00000419372.1:n.-3+27449G=
ENST00000547270.1:c.244C= (TAS2R38) MANE Select ENSP00000448219.1:p.Gln82=
NM_176817.4:c.244C= (TAS2R38) NP_789787.4:p.Gln82=
XM_011515783.1:c.*25-12950G= (OR9A4) XP_011514085.1:n.*25-12950G=
NM_176817.5:c.244C= (TAS2R38) MANE Select NP_789787.5:p.Gln82=