Canonical Allele Identifier: CA1928694494

Linked Data

dbSNP Id: rs2058308158

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93597197T>C , CM000672.2:g.93597197T>C GRCh38
NC_000010.10:g.95356954T>C , CM000672.1:g.95356954T>C GRCh37
NC_000010.9:g.95346944T>C NCBI36
NG_009104.1:g.9040A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371464.8:c.356-3162A>G (RBP4) MANE Select ENSP00000360519.3:n.356-3162A>G
ENST00000371464.7:c.356-3162A>G (RBP4) ENSP00000360519.3:n.356-3162A>G
ENST00000371467.5:c.356-3162A>G (RBP4) ENSP00000360522.1:n.356-3162A>G
ENST00000371469.2:c.350-3162A>G (RBP4) ENSP00000360524.2:n.350-3162A>G
ENST00000604414.1:c.697-6877T>C (FFAR4) ENSP00000474477.1:n.697-6877T>C
ENST00000615669.4:c.350-3162A>G (RBP4) ENSP00000480654.1:n.350-3162A>G
ENST00000629763.2:c.350-3162A>G (RBP4) ENSP00000487033.1:n.350-3162A>G
NM_006744.3:c.356-3162A>G (RBP4) NP_006735.2:n.356-3162A>G
NM_001323517.1:c.356-3162A>G (RBP4) NP_001310446.1:n.356-3162A>G
NM_001323518.1:c.350-3162A>G (RBP4) NP_001310447.1:n.350-3162A>G
NM_006744.4:c.356-3162A>G (RBP4) MANE Select NP_006735.2:n.356-3162A>G
NM_001323518.2:c.350-3162A>G (RBP4) NP_001310447.1:n.350-3162A>G