Canonical Allele Identifier: CA4520249
Gene: MGAM HGNC NCBI
TAS2R38 HGNC NCBI
OR9A4 HGNC NCBI

Linked Data

dbSNP Id: rs782526937
ExAC: 7:141673377 A / G
gnomAD v2: 7-141673377-A-G
gnomAD v4: 7-141973577-A-G
MyVariant Identifiers: chr7:g.141673377A>G (hg19) chr7:g.141973577A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973577A>G , CM000669.2:g.141973577A>G GRCh38
NC_000007.13:g.141673377A>G , CM000669.1:g.141673377A>G GRCh37
NC_000007.12:g.141319846A>G NCBI36
NG_016141.1:g.5197T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000465654.5:c.-3+27580A>G (MGAM) ENSP00000419372.1:n.-3+27580A>G
ENST00000547270.1:c.113T>C (TAS2R38) MANE Select ENSP00000448219.1:p.Leu38Ser
NM_176817.4:c.113T>C (TAS2R38) NP_789787.4:p.Leu38Ser
XM_011515783.1:c.*25-12819A>G (OR9A4) XP_011514085.1:n.*25-12819A>G
NM_176817.5:c.113T>C (TAS2R38) MANE Select NP_789787.5:p.Leu38Ser
Search 100 bp 5'
Search 100 bp 3'