Canonical Allele Identifier: CA168094861

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973938A>G , CM000669.2:g.141973938A>G GRCh38
NC_000007.13:g.141673738A>G , CM000669.1:g.141673738A>G GRCh37
NC_000007.12:g.141320207A>G NCBI36
NG_016141.1:g.4836T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27941A>G (MGAM) ENSP00000419372.1:n.-3+27941A>G
XM_011515783.1:c.*25-12458A>G (OR9A4) XP_011514085.1:n.*25-12458A>G