Canonical Allele Identifier: CA2610205381
Gene: FFAR4 HGNC NCBI

Linked Data

gnomAD v4: 10-93588335-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93588335A>G , CM000672.2:g.93588335A>G GRCh38
NC_000010.10:g.95348092A>G , CM000672.1:g.95348092A>G GRCh37
NC_000010.9:g.95338082A>G NCBI36
NG_032670.1:g.26671A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371481.9:c.*726A>G MANE Select ENSP00000360536.5:n.*726A>G
ENST00000371481.8:c.*726A>G ENSP00000360536.4:n.*726A>G
ENST00000371483.8:c.*726A>G ENSP00000360538.4:n.*726A>G
ENST00000604414.1:c.696+12116A>G ENSP00000474477.1:n.696+12116A>G
NM_001195755.1:c.*726A>G NP_001182684.1:n.*726A>G
NM_181745.3:c.*726A>G NP_859529.2:n.*726A>G
NM_001195755.2:c.*726A>G MANE Select NP_001182684.1:n.*726A>G
NM_181745.4:c.*726A>G NP_859529.2:n.*726A>G
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