Canonical Allele Identifier: CA369564299

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141972977C>G , CM000669.2:g.141972977C>G GRCh38
NC_000007.13:g.141672777C>G , CM000669.1:g.141672777C>G GRCh37
NC_000007.12:g.141319246C>G NCBI36
NG_016141.1:g.5797G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+26980C>G (MGAM) ENSP00000419372.1:n.-3+26980C>G
ENST00000547270.1:c.713G>C (TAS2R38) MANE Select ENSP00000448219.1:p.Ser238Thr
NM_176817.4:c.713G>C (TAS2R38) NP_789787.4:p.Ser238Thr
XM_011515783.1:c.*25-13419C>G (OR9A4) XP_011514085.1:n.*25-13419C>G
NM_176817.5:c.713G>C (TAS2R38) MANE Select NP_789787.5:p.Ser238Thr