Canonical Allele Identifier: CA2579045739

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973762A>C , CM000669.2:g.141973762A>C GRCh38
NC_000007.13:g.141673562A>C , CM000669.1:g.141673562A>C GRCh37
NC_000007.12:g.141320031A>C NCBI36
NG_016141.1:g.5012T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27765A>C (MGAM) ENSP00000419372.1:n.-3+27765A>C
ENST00000547270.1:c.-73T>G (TAS2R38) MANE Select ENSP00000448219.1:n.-73T>G
NM_176817.4:c.-73T>G (TAS2R38) NP_789787.4:n.-73T>G
XM_011515783.1:c.*25-12634A>C (OR9A4) XP_011514085.1:n.*25-12634A>C
NM_176817.5:c.-73T>G (TAS2R38) MANE Select NP_789787.5:n.-73T>G