Canonical Allele Identifier: CA2685283405

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141972619T>C , CM000669.2:g.141972619T>C GRCh38
NC_000007.13:g.141672419T>C , CM000669.1:g.141672419T>C GRCh37
NC_000007.12:g.141318888T>C NCBI36
NG_016141.1:g.6155A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+26622T>C (MGAM) ENSP00000419372.1:n.-3+26622T>C
XM_011515783.1:c.*25-13777T>C (OR9A4) XP_011514085.1:n.*25-13777T>C