Canonical Allele Identifier: CA2685283414

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141972633C>A , CM000669.2:g.141972633C>A GRCh38
NC_000007.13:g.141672433C>A , CM000669.1:g.141672433C>A GRCh37
NC_000007.12:g.141318902C>A NCBI36
NG_016141.1:g.6141G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000465654.5:c.-3+26636C>A (MGAM) ENSP00000419372.1:n.-3+26636C>A
ENST00000547270.1:c.*55G>T (TAS2R38) MANE Select ENSP00000448219.1:n.*55G>T
NM_176817.4:c.*55G>T (TAS2R38) NP_789787.4:n.*55G>T
XM_011515783.1:c.*25-13763C>A (OR9A4) XP_011514085.1:n.*25-13763C>A
NM_176817.5:c.*55G>T (TAS2R38) MANE Select NP_789787.5:n.*55G>T