Canonical Allele Identifier: CA2515845096

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973989T>A , CM000669.2:g.141973989T>A GRCh38
NC_000007.13:g.141673789T>A , CM000669.1:g.141673789T>A GRCh37
NC_000007.12:g.141320258T>A NCBI36
NG_016141.1:g.4785A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27992T>A (MGAM) ENSP00000419372.1:n.-3+27992T>A
XM_011515783.1:c.*25-12407T>A (OR9A4) XP_011514085.1:n.*25-12407T>A