Canonical Allele Identifier: CA369564349

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973001T>G , CM000669.2:g.141973001T>G GRCh38
NC_000007.13:g.141672801T>G , CM000669.1:g.141672801T>G GRCh37
NC_000007.12:g.141319270T>G NCBI36
NG_016141.1:g.5773A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27004T>G (MGAM) ENSP00000419372.1:n.-3+27004T>G
ENST00000547270.1:c.689A>C (TAS2R38) MANE Select ENSP00000448219.1:p.Tyr230Ser
NM_176817.4:c.689A>C (TAS2R38) NP_789787.4:p.Tyr230Ser
XM_011515783.1:c.*25-13395T>G (OR9A4) XP_011514085.1:n.*25-13395T>G
NM_176817.5:c.689A>C (TAS2R38) MANE Select NP_789787.5:p.Tyr230Ser