Canonical Allele Identifier: CA369565889

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973496A>G , CM000669.2:g.141973496A>G GRCh38
NC_000007.13:g.141673296A>G , CM000669.1:g.141673296A>G GRCh37
NC_000007.12:g.141319765A>G NCBI36
NG_016141.1:g.5278T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27499A>G (MGAM) ENSP00000419372.1:n.-3+27499A>G
ENST00000547270.1:c.194T>C (TAS2R38) MANE Select ENSP00000448219.1:p.Leu65Pro
NM_176817.4:c.194T>C (TAS2R38) NP_789787.4:p.Leu65Pro
XM_011515783.1:c.*25-12900A>G (OR9A4) XP_011514085.1:n.*25-12900A>G
NM_176817.5:c.194T>C (TAS2R38) MANE Select NP_789787.5:p.Leu65Pro