Canonical Allele Identifier: CA2610208264
Gene: FFAR4 HGNC NCBI

Linked Data

gnomAD v4: 10-93588282-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93588282T>A , CM000672.2:g.93588282T>A GRCh38
NC_000010.10:g.95348039T>A , CM000672.1:g.95348039T>A GRCh37
NC_000010.9:g.95338029T>A NCBI36
NG_032670.1:g.26618T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371481.9:c.*673T>A MANE Select ENSP00000360536.5:n.*673T>A
ENST00000371481.8:c.*673T>A ENSP00000360536.4:n.*673T>A
ENST00000371483.8:c.*673T>A ENSP00000360538.4:n.*673T>A
ENST00000604414.1:c.696+12063T>A ENSP00000474477.1:n.696+12063T>A
NM_001195755.1:c.*673T>A NP_001182684.1:n.*673T>A
NM_181745.3:c.*673T>A NP_859529.2:n.*673T>A
NM_001195755.2:c.*673T>A MANE Select NP_001182684.1:n.*673T>A
NM_181745.4:c.*673T>A NP_859529.2:n.*673T>A
Search 100 bp 5'
Search 100 bp 3'