Canonical Allele Identifier: CA1748245561
Gene: MGAM HGNC NCBI
TAS2R38 HGNC NCBI
OR9A4 HGNC NCBI

Linked Data

dbSNP Id: rs1584866988
gnomAD v4: 7-141973772-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973772G>A , CM000669.2:g.141973772G>A GRCh38
NC_000007.13:g.141673572G>A , CM000669.1:g.141673572G>A GRCh37
NC_000007.12:g.141320041G>A NCBI36
NG_016141.1:g.5002C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27775G>A (MGAM) ENSP00000419372.1:n.-3+27775G>A
ENST00000547270.1:c.-83C>T (TAS2R38) MANE Select ENSP00000448219.1:n.-83C>T
NM_176817.4:c.-83C>T (TAS2R38) NP_789787.4:n.-83C>T
XM_011515783.1:c.*25-12624G>A (OR9A4) XP_011514085.1:n.*25-12624G>A
NM_176817.5:c.-83C>T (TAS2R38) MANE Select NP_789787.5:n.-83C>T
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