Canonical Allele Identifier: CA592244896
Gene: FRMD4A HGNC NCBI

Linked Data

dbSNP Id: rs1365139519
gnomAD v2: 10-14479007-A-G
gnomAD v3: 10-14437008-A-G
gnomAD v4: 10-14437008-A-G
MyVariant Identifiers: chr10:g.14479007A>G (hg19) chr10:g.14437008A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.14437008A>G , CM000672.2:g.14437008A>G GRCh38
NC_000010.10:g.14479007A>G , CM000672.1:g.14479007A>G GRCh37
NC_000010.9:g.14519013A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000475141.2:c.-305+25060T>C ENSP00000473870.1:n.-305+25060T>C
ENST00000493380.5:c.-82+25060T>C ENSP00000474863.1:n.-82+25060T>C
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