Canonical Allele Identifier: CA13386512
Gene: FGF4 HGNC NCBI
MyVariant.info:
GRCh38 chr11:g.69775191A>G
GRCh37 chr11:g.69589959A>G
gnomAD v2:
11:69589959 A / G
gnomAD v3:
11:69775191 A / G
gnomAD v4:
chr11-69775191-A-G
Joint Max Group AF 0.68014201 (EAS)
Genomes Max Group AF 0.72368968 (EAS)
Exomes Max Group AF 0.67029673 (AMR)
dbSNP:
9666584
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69775191A>G , CM000673.2:g.69775191A>G GRCh38
NC_000011.9:g.69589959A>G , CM000673.1:g.69589959A>G GRCh37
NC_000011.8:g.69299140A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000168712.3:c.-107T>C MANE Select ENSP00000168712.1:n.-107T>C
ENST00000168712.2:c.-107T>C ENSP00000168712.1:n.-107T>C
NM_002007.2:c.-107T>C NP_001998.1:n.-107T>C
NM_002007.3:c.-107T>C NP_001998.1:n.-107T>C
NM_002007.4:c.-107T>C MANE Select NP_001998.1:n.-107T>C
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