Canonical Allele Identifier: CA1748245197
Gene: MGAM HGNC NCBI
TAS2R38 HGNC NCBI
OR9A4 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973483T= , CM000669.2:g.141973483T= GRCh38
NC_000007.13:g.141673283T= , CM000669.1:g.141673283T= GRCh37
NC_000007.12:g.141319752T= NCBI36
NG_016141.1:g.5291A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27486T= (MGAM) ENSP00000419372.1:n.-3+27486T=
ENST00000547270.1:c.207A= (TAS2R38) MANE Select ENSP00000448219.1:p.Gly69=
NM_176817.4:c.207A= (TAS2R38) NP_789787.4:p.Gly69=
XM_011515783.1:c.*25-12913T= (OR9A4) XP_011514085.1:n.*25-12913T=
NM_176817.5:c.207A= (TAS2R38) MANE Select NP_789787.5:p.Gly69=
Search 100 bp 5'
Search 100 bp 3'