Canonical Allele Identifier: CA168094799

Linked Data

dbSNP Id: rs2115240005

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973839C>G , CM000669.2:g.141973839C>G GRCh38
NC_000007.13:g.141673639C>G , CM000669.1:g.141673639C>G GRCh37
NC_000007.12:g.141320108C>G NCBI36
NG_016141.1:g.4935G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27842C>G (MGAM) ENSP00000419372.1:n.-3+27842C>G
XM_011515783.1:c.*25-12557C>G (OR9A4) XP_011514085.1:n.*25-12557C>G