Canonical Allele Identifier: CA211546457
Gene: FFAR4 HGNC NCBI

Linked Data

dbSNP Id: rs909985718
gnomAD v2: 10-95348078-C-T
gnomAD v3: 10-93588321-C-T
gnomAD v4: 10-93588321-C-T
MyVariant Identifiers: chr10:g.95348078C>T (hg19) chr10:g.93588321C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93588321C>T , CM000672.2:g.93588321C>T GRCh38
NC_000010.10:g.95348078C>T , CM000672.1:g.95348078C>T GRCh37
NC_000010.9:g.95338068C>T NCBI36
NG_032670.1:g.26657C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371481.9:c.*712C>T MANE Select ENSP00000360536.5:n.*712C>T
ENST00000371481.8:c.*712C>T ENSP00000360536.4:n.*712C>T
ENST00000371483.8:c.*712C>T ENSP00000360538.4:n.*712C>T
ENST00000604414.1:c.696+12102C>T ENSP00000474477.1:n.696+12102C>T
NM_001195755.1:c.*712C>T NP_001182684.1:n.*712C>T
NM_181745.3:c.*712C>T NP_859529.2:n.*712C>T
NM_001195755.2:c.*712C>T MANE Select NP_001182684.1:n.*712C>T
NM_181745.4:c.*712C>T NP_859529.2:n.*712C>T
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