Canonical Allele Identifier: CA369564222

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141972942C>A , CM000669.2:g.141972942C>A GRCh38
NC_000007.13:g.141672742C>A , CM000669.1:g.141672742C>A GRCh37
NC_000007.12:g.141319211C>A NCBI36
NG_016141.1:g.5832G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+26945C>A (MGAM) ENSP00000419372.1:n.-3+26945C>A
ENST00000547270.1:c.748G>T (TAS2R38) MANE Select ENSP00000448219.1:p.Val250Phe
NM_176817.4:c.748G>T (TAS2R38) NP_789787.4:p.Val250Phe
XM_011515783.1:c.*25-13454C>A (OR9A4) XP_011514085.1:n.*25-13454C>A
NM_176817.5:c.748G>T (TAS2R38) MANE Select NP_789787.5:p.Val250Phe