Canonical Allele Identifier: CA595270140

Gene: FFAR4

Linked Data

• dbSNP Id: rs12415204
• gnomAD v2: 10-95330890-C-T
• gnomAD v3: 10-93571133-C-T
• gnomAD v4: 10-93571133-C-T
• MyVariant Identifiers: chr10:g.95330890C>T (hg19) ; chr10:g.93571133C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93571133C>T , CM000672.2:g.93571133C>T	GRCh38
NC_000010.10:g.95330890C>T , CM000672.1:g.95330890C>T	GRCh37
NC_000010.9:g.95320880C>T	NCBI36
NG_032670.1:g.9469C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371481.9:c.567+3846C>T MANE Select	ENSP00000360536.5:n.567+3846C>T
ENST00000371481.8:c.567+3846C>T	ENSP00000360536.4:n.567+3846C>T
ENST00000371483.8:c.567+3846C>T	ENSP00000360538.4:n.567+3846C>T
ENST00000604414.1:c.567+3846C>T	ENSP00000474477.1:n.567+3846C>T
NM_001195755.1:c.567+3846C>T	NP_001182684.1:n.567+3846C>T
NM_181745.3:c.567+3846C>T	NP_859529.2:n.567+3846C>T
XM_011539746.1:c.567+3846C>T	XP_011538048.1:n.567+3846C>T
XM_011539746.3:c.567+3846C>T	XP_011538048.1:n.567+3846C>T
NM_001195755.2:c.567+3846C>T MANE Select	NP_001182684.1:n.567+3846C>T
NM_181745.4:c.567+3846C>T	NP_859529.2:n.567+3846C>T