Canonical Allele Identifier: CA1748245082

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973382T= , CM000669.2:g.141973382T= GRCh38
NC_000007.13:g.141673182T= , CM000669.1:g.141673182T= GRCh37
NC_000007.12:g.141319651T= NCBI36
NG_016141.1:g.5392A=

Transcript Alleles

HGVS Amino-acid change
ENST00000465654.5:c.-3+27385T= (MGAM) ENSP00000419372.1:n.-3+27385T=
ENST00000547270.1:c.308A= (TAS2R38) MANE Select ENSP00000448219.1:p.Asn103=
NM_176817.4:c.308A= (TAS2R38) NP_789787.4:p.Asn103=
XM_011515783.1:c.*25-13014T= (OR9A4) XP_011514085.1:n.*25-13014T=
NM_176817.5:c.308A= (TAS2R38) MANE Select NP_789787.5:p.Asn103=