Canonical Allele Identifier: CA1748245736

Linked Data

dbSNP Id: rs1803414925

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973967del , CM000669.2:g.141973967del GRCh38
NC_000007.13:g.141673767del , CM000669.1:g.141673767del GRCh37
NC_000007.12:g.141320236del NCBI36
NG_016141.1:g.4807del

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27970del (MGAM) ENSP00000419372.1:n.-3+27970del
XM_011515783.1:c.*25-12429del (OR9A4) XP_011514085.1:n.*25-12429del