Canonical Allele Identifier: CA1928689091
Gene: FFAR4 HGNC NCBI

Linked Data

dbSNP Id: rs2058242265
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93588330T>G , CM000672.2:g.93588330T>G GRCh38
NC_000010.10:g.95348087T>G , CM000672.1:g.95348087T>G GRCh37
NC_000010.9:g.95338077T>G NCBI36
NG_032670.1:g.26666T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371481.9:c.*721T>G MANE Select ENSP00000360536.5:n.*721T>G
ENST00000371481.8:c.*721T>G ENSP00000360536.4:n.*721T>G
ENST00000371483.8:c.*721T>G ENSP00000360538.4:n.*721T>G
ENST00000604414.1:c.696+12111T>G ENSP00000474477.1:n.696+12111T>G
NM_001195755.1:c.*721T>G NP_001182684.1:n.*721T>G
NM_181745.3:c.*721T>G NP_859529.2:n.*721T>G
NM_001195755.2:c.*721T>G MANE Select NP_001182684.1:n.*721T>G
NM_181745.4:c.*721T>G NP_859529.2:n.*721T>G
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