Canonical Allele Identifier: CA1108025749

Linked Data

dbSNP Id: rs1554444502

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973960G>C , CM000669.2:g.141973960G>C GRCh38
NC_000007.13:g.141673760G>C , CM000669.1:g.141673760G>C GRCh37
NC_000007.12:g.141320229G>C NCBI36
NG_016141.1:g.4814C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27963G>C (MGAM) ENSP00000419372.1:n.-3+27963G>C
XM_011515783.1:c.*25-12436G>C (OR9A4) XP_011514085.1:n.*25-12436G>C