Canonical Allele Identifier: CA578290167
Gene: MGAM HGNC NCBI
TAS2R38 HGNC NCBI
OR9A4 HGNC NCBI

Linked Data

dbSNP Id: rs1554444304
gnomAD v2: 7-141672449-C-G
gnomAD v4: 7-141972649-C-G
MyVariant Identifiers: chr7:g.141672449C>G (hg19) chr7:g.141972649C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141972649C>G , CM000669.2:g.141972649C>G GRCh38
NC_000007.13:g.141672449C>G , CM000669.1:g.141672449C>G GRCh37
NC_000007.12:g.141318918C>G NCBI36
NG_016141.1:g.6125G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000465654.5:c.-3+26652C>G (MGAM) ENSP00000419372.1:n.-3+26652C>G
ENST00000547270.1:c.*39G>C (TAS2R38) MANE Select ENSP00000448219.1:n.*39G>C
NM_176817.4:c.*39G>C (TAS2R38) NP_789787.4:n.*39G>C
XM_011515783.1:c.*25-13747C>G (OR9A4) XP_011514085.1:n.*25-13747C>G
NM_176817.5:c.*39G>C (TAS2R38) MANE Select NP_789787.5:n.*39G>C
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