Canonical Allele Identifier: CA2685283571

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973898dup , CM000669.2:g.141973898dup GRCh38
NC_000007.13:g.141673698dup , CM000669.1:g.141673698dup GRCh37
NC_000007.12:g.141320167dup NCBI36
NG_016141.1:g.4877dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27901dup (MGAM) ENSP00000419372.1:n.-3+27901dup
XM_011515783.1:c.*25-12498dup (OR9A4) XP_011514085.1:n.*25-12498dup