Canonical Allele Identifier: CA670062020

Gene: RBP4 FFAR4

Linked Data

• dbSNP Id: rs1344289179
• gnomAD v3: 10-93597205-G-C
• gnomAD v4: 10-93597205-G-C
• MyVariant Identifiers: chr10:g.95356962G>C (hg19) ; chr10:g.93597205G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93597205G>C , CM000672.2:g.93597205G>C	GRCh38
NC_000010.10:g.95356962G>C , CM000672.1:g.95356962G>C	GRCh37
NC_000010.9:g.95346952G>C	NCBI36
NG_009104.1:g.9032C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371464.8:c.356-3170C>G (RBP4) MANE Select	ENSP00000360519.3:n.356-3170C>G
ENST00000371464.7:c.356-3170C>G (RBP4)	ENSP00000360519.3:n.356-3170C>G
ENST00000371467.5:c.356-3170C>G (RBP4)	ENSP00000360522.1:n.356-3170C>G
ENST00000371469.2:c.350-3170C>G (RBP4)	ENSP00000360524.2:n.350-3170C>G
ENST00000604414.1:c.697-6869G>C (FFAR4)	ENSP00000474477.1:n.697-6869G>C
ENST00000615669.4:c.350-3170C>G (RBP4)	ENSP00000480654.1:n.350-3170C>G
ENST00000629763.2:c.350-3170C>G (RBP4)	ENSP00000487033.1:n.350-3170C>G
NM_006744.3:c.356-3170C>G (RBP4)	NP_006735.2:n.356-3170C>G
NM_001323517.1:c.356-3170C>G (RBP4)	NP_001310446.1:n.356-3170C>G
NM_001323518.1:c.350-3170C>G (RBP4)	NP_001310447.1:n.350-3170C>G
NM_006744.4:c.356-3170C>G (RBP4) MANE Select	NP_006735.2:n.356-3170C>G
NM_001323518.2:c.350-3170C>G (RBP4)	NP_001310447.1:n.350-3170C>G