Canonical Allele Identifier: CA595271515
Gene: FFAR4 HGNC NCBI

Linked Data

dbSNP Id: rs1269518694
gnomAD v2: 10-95348168-A-T
gnomAD v3: 10-93588411-A-T
gnomAD v4: 10-93588411-A-T
MyVariant Identifiers: chr10:g.95348168A>T (hg19) chr10:g.93588411A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93588411A>T , CM000672.2:g.93588411A>T GRCh38
NC_000010.10:g.95348168A>T , CM000672.1:g.95348168A>T GRCh37
NC_000010.9:g.95338158A>T NCBI36
NG_032670.1:g.26747A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371481.9:c.*802A>T MANE Select ENSP00000360536.5:n.*802A>T
ENST00000371481.8:c.*802A>T ENSP00000360536.4:n.*802A>T
ENST00000371483.8:c.*802A>T ENSP00000360538.4:n.*802A>T
ENST00000604414.1:c.696+12192A>T ENSP00000474477.1:n.696+12192A>T
NM_001195755.1:c.*802A>T NP_001182684.1:n.*802A>T
NM_181745.3:c.*802A>T NP_859529.2:n.*802A>T
NM_001195755.2:c.*802A>T MANE Select NP_001182684.1:n.*802A>T
NM_181745.4:c.*802A>T NP_859529.2:n.*802A>T
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