Canonical Allele Identifier: CA369564892

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973232A>C , CM000669.2:g.141973232A>C GRCh38
NC_000007.13:g.141673032A>C , CM000669.1:g.141673032A>C GRCh37
NC_000007.12:g.141319501A>C NCBI36
NG_016141.1:g.5542T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27235A>C (MGAM) ENSP00000419372.1:n.-3+27235A>C
ENST00000547270.1:c.458T>G (TAS2R38) MANE Select ENSP00000448219.1:p.Ile153Ser
NM_176817.4:c.458T>G (TAS2R38) NP_789787.4:p.Ile153Ser
XM_011515783.1:c.*25-13164A>C (OR9A4) XP_011514085.1:n.*25-13164A>C
NM_176817.5:c.458T>G (TAS2R38) MANE Select NP_789787.5:p.Ile153Ser