Canonical Allele Identifier: CA1928693818

Linked Data

dbSNP Id: rs2058341164

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93601735del , CM000672.2:g.93601735del GRCh38
NC_000010.10:g.95361492del , CM000672.1:g.95361492del GRCh37
NC_000010.9:g.95351482del NCBI36
NG_009104.1:g.4505del

Transcript Alleles

HGVS Amino-acid change
ENST00000371469.2:c.-16del (RBP4) ENSP00000360524.2:n.-16del
ENST00000604414.1:c.697-2339del (FFAR4) ENSP00000474477.1:n.697-2339del
NM_001323518.1:c.-16del (RBP4) NP_001310447.1:n.-16del
NM_001323518.2:c.-16del (RBP4) NP_001310447.1:n.-16del