Canonical Allele Identifier: CA369563687

Linked Data

dbSNP Id: rs1554444331

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141972788T>C , CM000669.2:g.141972788T>C GRCh38
NC_000007.13:g.141672588T>C , CM000669.1:g.141672588T>C GRCh37
NC_000007.12:g.141319057T>C NCBI36
NG_016141.1:g.5986A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+26791T>C (MGAM) ENSP00000419372.1:n.-3+26791T>C
ENST00000547270.1:c.902A>G (TAS2R38) MANE Select ENSP00000448219.1:p.Asn301Ser
NM_176817.4:c.902A>G (TAS2R38) NP_789787.4:p.Asn301Ser
XM_011515783.1:c.*25-13608T>C (OR9A4) XP_011514085.1:n.*25-13608T>C
NM_176817.5:c.902A>G (TAS2R38) MANE Select NP_789787.5:p.Asn301Ser