Canonical Allele Identifier: CA670081965

Gene: FFAR4

Linked Data

• dbSNP Id: rs1256647352
• gnomAD v3: 10-93588423-G-T
• gnomAD v4: 10-93588423-G-T
• MyVariant Identifiers: chr10:g.95348180G>T (hg19) ; chr10:g.93588423G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93588423G>T , CM000672.2:g.93588423G>T	GRCh38
NC_000010.10:g.95348180G>T , CM000672.1:g.95348180G>T	GRCh37
NC_000010.9:g.95338170G>T	NCBI36
NG_032670.1:g.26759G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371481.9:c.*814G>T MANE Select	ENSP00000360536.5:n.*814G>T
ENST00000371481.8:c.*814G>T	ENSP00000360536.4:n.*814G>T
ENST00000371483.8:c.*814G>T	ENSP00000360538.4:n.*814G>T
ENST00000604414.1:c.696+12204G>T	ENSP00000474477.1:n.696+12204G>T
NM_001195755.1:c.*814G>T	NP_001182684.1:n.*814G>T
NM_181745.3:c.*814G>T	NP_859529.2:n.*814G>T
NM_001195755.2:c.*814G>T MANE Select	NP_001182684.1:n.*814G>T
NM_181745.4:c.*814G>T	NP_859529.2:n.*814G>T