Canonical Allele Identifier: CA2685283538

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973856A>C , CM000669.2:g.141973856A>C GRCh38
NC_000007.13:g.141673656A>C , CM000669.1:g.141673656A>C GRCh37
NC_000007.12:g.141320125A>C NCBI36
NG_016141.1:g.4918T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27859A>C (MGAM) ENSP00000419372.1:n.-3+27859A>C
XM_011515783.1:c.*25-12540A>C (OR9A4) XP_011514085.1:n.*25-12540A>C