Canonical Allele Identifier: CA369565360

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973368A>C , CM000669.2:g.141973368A>C GRCh38
NC_000007.13:g.141673168A>C , CM000669.1:g.141673168A>C GRCh37
NC_000007.12:g.141319637A>C NCBI36
NG_016141.1:g.5406T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000465654.5:c.-3+27371A>C (MGAM) ENSP00000419372.1:n.-3+27371A>C
ENST00000547270.1:c.322T>G (TAS2R38) MANE Select ENSP00000448219.1:p.Trp108Gly
NM_176817.4:c.322T>G (TAS2R38) NP_789787.4:p.Trp108Gly
XM_011515783.1:c.*25-13028A>C (OR9A4) XP_011514085.1:n.*25-13028A>C
NM_176817.5:c.322T>G (TAS2R38) MANE Select NP_789787.5:p.Trp108Gly