Canonical Allele Identifier: CA4520103

Linked Data

dbSNP Id: rs368826009

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141972656G>A , CM000669.2:g.141972656G>A GRCh38
NC_000007.13:g.141672456G>A , CM000669.1:g.141672456G>A GRCh37
NC_000007.12:g.141318925G>A NCBI36
NG_016141.1:g.6118C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+26659G>A (MGAM) ENSP00000419372.1:n.-3+26659G>A
ENST00000547270.1:c.*32C>T (TAS2R38) MANE Select ENSP00000448219.1:n.*32C>T
NM_176817.4:c.*32C>T (TAS2R38) NP_789787.4:n.*32C>T
XM_011515783.1:c.*25-13740G>A (OR9A4) XP_011514085.1:n.*25-13740G>A
NM_176817.5:c.*32C>T (TAS2R38) MANE Select NP_789787.5:n.*32C>T