Canonical Allele Identifier: CA115857
Gene: MGAM HGNC NCBI
TAS2R38 HGNC NCBI
OR9A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.141672705G>G (hg19) chr7:g.141972905G>G (hg38)
PubMed: PMID:12595690
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141972905G= , CM000669.2:g.141972905G= GRCh38
NC_000007.13:g.141672705G= , CM000669.1:g.141672705G= GRCh37
NC_000007.12:g.141319174G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+26908G= (MGAM) ENSP00000419372.1:n.-3+26908G=
ENST00000547270.1:c.785C= (TAS2R38) MANE Select ENSP00000448219.1:p.Ala262=
XM_011515783.1:c.*25-13491G= (OR9A4) XP_011514085.1:n.*25-13491G=
NM_176817.5:c.785C= (TAS2R38) MANE Select NP_789787.5:p.Ala262=
Search 100 bp 5'
Search 100 bp 3'