Canonical Allele Identifier: CA1748244569
Gene: MGAM HGNC NCBI
TAS2R38 HGNC NCBI
OR9A4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973015C= , CM000669.2:g.141973015C= GRCh38
NC_000007.13:g.141672815C= , CM000669.1:g.141672815C= GRCh37
NC_000007.12:g.141319284C= NCBI36
NG_016141.1:g.5759G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27018C= (MGAM) ENSP00000419372.1:n.-3+27018C=
ENST00000547270.1:c.675G= (TAS2R38) MANE Select ENSP00000448219.1:p.Arg225=
NM_176817.4:c.675G= (TAS2R38) NP_789787.4:p.Arg225=
XM_011515783.1:c.*25-13381C= (OR9A4) XP_011514085.1:n.*25-13381C=
NM_176817.5:c.675G= (TAS2R38) MANE Select NP_789787.5:p.Arg225=
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