Canonical Allele Identifier: CA369565075

Linked Data

dbSNP Id: rs1803401032

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973301A>G , CM000669.2:g.141973301A>G GRCh38
NC_000007.13:g.141673101A>G , CM000669.1:g.141673101A>G GRCh37
NC_000007.12:g.141319570A>G NCBI36
NG_016141.1:g.5473T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27304A>G (MGAM) ENSP00000419372.1:n.-3+27304A>G
ENST00000547270.1:c.389T>C (TAS2R38) MANE Select ENSP00000448219.1:p.Ile130Thr
NM_176817.4:c.389T>C (TAS2R38) NP_789787.4:p.Ile130Thr
XM_011515783.1:c.*25-13095A>G (OR9A4) XP_011514085.1:n.*25-13095A>G
NM_176817.5:c.389T>C (TAS2R38) MANE Select NP_789787.5:p.Ile130Thr