Canonical Allele Identifier: CA1748245708

Linked Data

dbSNP Id: rs1803414406

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973947G>T , CM000669.2:g.141973947G>T GRCh38
NC_000007.13:g.141673747G>T , CM000669.1:g.141673747G>T GRCh37
NC_000007.12:g.141320216G>T NCBI36
NG_016141.1:g.4827C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27950G>T (MGAM) ENSP00000419372.1:n.-3+27950G>T
XM_011515783.1:c.*25-12449G>T (OR9A4) XP_011514085.1:n.*25-12449G>T