Canonical Allele Identifier: CA369566435

Linked Data

dbSNP Id: rs1398780610

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973658G>A , CM000669.2:g.141973658G>A GRCh38
NC_000007.13:g.141673458G>A , CM000669.1:g.141673458G>A GRCh37
NC_000007.12:g.141319927G>A NCBI36
NG_016141.1:g.5116C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27661G>A (MGAM) ENSP00000419372.1:n.-3+27661G>A
ENST00000547270.1:c.32C>T (TAS2R38) MANE Select ENSP00000448219.1:p.Ser11Phe
NM_176817.4:c.32C>T (TAS2R38) NP_789787.4:p.Ser11Phe
XM_011515783.1:c.*25-12738G>A (OR9A4) XP_011514085.1:n.*25-12738G>A
NM_176817.5:c.32C>T (TAS2R38) MANE Select NP_789787.5:p.Ser11Phe