Canonical Allele Identifier: CA369565635

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973444C>G , CM000669.2:g.141973444C>G GRCh38
NC_000007.13:g.141673244C>G , CM000669.1:g.141673244C>G GRCh37
NC_000007.12:g.141319713C>G NCBI36
NG_016141.1:g.5330G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27447C>G (MGAM) ENSP00000419372.1:n.-3+27447C>G
ENST00000547270.1:c.246G>C (TAS2R38) MANE Select ENSP00000448219.1:p.Gln82His
NM_176817.4:c.246G>C (TAS2R38) NP_789787.4:p.Gln82His
XM_011515783.1:c.*25-12952C>G (OR9A4) XP_011514085.1:n.*25-12952C>G
NM_176817.5:c.246G>C (TAS2R38) MANE Select NP_789787.5:p.Gln82His