Canonical Allele Identifier: CA1748244632

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973047T= , CM000669.2:g.141973047T= GRCh38
NC_000007.13:g.141672847T= , CM000669.1:g.141672847T= GRCh37
NC_000007.12:g.141319316T= NCBI36
NG_016141.1:g.5727A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27050T= (MGAM) ENSP00000419372.1:n.-3+27050T=
ENST00000547270.1:c.643A= (TAS2R38) MANE Select ENSP00000448219.1:p.Met215=
NM_176817.4:c.643A= (TAS2R38) NP_789787.4:p.Met215=
XM_011515783.1:c.*25-13349T= (OR9A4) XP_011514085.1:n.*25-13349T=
NM_176817.5:c.643A= (TAS2R38) MANE Select NP_789787.5:p.Met215=