Canonical Allele Identifier: CA369565000
Gene: MGAM HGNC NCBI
TAS2R38 HGNC NCBI
OR9A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.141673081A>T (hg19) chr7:g.141973281A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973281A>T , CM000669.2:g.141973281A>T GRCh38
NC_000007.13:g.141673081A>T , CM000669.1:g.141673081A>T GRCh37
NC_000007.12:g.141319550A>T NCBI36
NG_016141.1:g.5493T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000465654.5:c.-3+27284A>T (MGAM) ENSP00000419372.1:n.-3+27284A>T
ENST00000547270.1:c.409T>A (TAS2R38) MANE Select ENSP00000448219.1:p.Ser137Thr
NM_176817.4:c.409T>A (TAS2R38) NP_789787.4:p.Ser137Thr
XM_011515783.1:c.*25-13115A>T (OR9A4) XP_011514085.1:n.*25-13115A>T
NM_176817.5:c.409T>A (TAS2R38) MANE Select NP_789787.5:p.Ser137Thr
Search 100 bp 5'
Search 100 bp 3'