Canonical Allele Identifier: CA458161429

Linked Data

MyVariant Identifiers: chr7:g.141673427A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973627A>G , CM000669.2:g.141973627A>G GRCh38
NC_000007.13:g.141673427A>G , CM000669.1:g.141673427A>G GRCh37
NC_000007.12:g.141319896A>G NCBI36
NG_016141.1:g.5147T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27630A>G (MGAM) ENSP00000419372.1:n.-3+27630A>G
ENST00000547270.1:c.63T>C (TAS2R38) MANE Select ENSP00000448219.1:p.Ile21=
NM_176817.4:c.63T>C (TAS2R38) NP_789787.4:p.Ile21=
XM_011515783.1:c.*25-12769A>G (OR9A4) XP_011514085.1:n.*25-12769A>G
NM_176817.5:c.63T>C (TAS2R38) MANE Select NP_789787.5:p.Ile21=