Canonical Allele Identifier: CA369565738

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973474G>C , CM000669.2:g.141973474G>C GRCh38
NC_000007.13:g.141673274G>C , CM000669.1:g.141673274G>C GRCh37
NC_000007.12:g.141319743G>C NCBI36
NG_016141.1:g.5300C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000465654.5:c.-3+27477G>C (MGAM) ENSP00000419372.1:n.-3+27477G>C
ENST00000547270.1:c.216C>G (TAS2R38) MANE Select ENSP00000448219.1:p.Phe72Leu
NM_176817.4:c.216C>G (TAS2R38) NP_789787.4:p.Phe72Leu
XM_011515783.1:c.*25-12922G>C (OR9A4) XP_011514085.1:n.*25-12922G>C
NM_176817.5:c.216C>G (TAS2R38) MANE Select NP_789787.5:p.Phe72Leu