Canonical Allele Identifier: CA1108025761

Linked Data

dbSNP Id: rs1803415473

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973981C>A , CM000669.2:g.141973981C>A GRCh38
NC_000007.13:g.141673781C>A , CM000669.1:g.141673781C>A GRCh37
NC_000007.12:g.141320250C>A NCBI36
NG_016141.1:g.4793G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27984C>A (MGAM) ENSP00000419372.1:n.-3+27984C>A
XM_011515783.1:c.*25-12415C>A (OR9A4) XP_011514085.1:n.*25-12415C>A