Canonical Allele Identifier: CA203746044
Gene: FRMD4A HGNC NCBI

Linked Data

dbSNP Id: rs551350856
gnomAD v3: 10-14437026-T-G
gnomAD v4: 10-14437026-T-G
MyVariant Identifiers: chr10:g.14479025T>G (hg19) chr10:g.14437026T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.14437026T>G , CM000672.2:g.14437026T>G GRCh38
NC_000010.10:g.14479025T>G , CM000672.1:g.14479025T>G GRCh37
NC_000010.9:g.14519031T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000475141.2:c.-305+25042A>C ENSP00000473870.1:n.-305+25042A>C
ENST00000493380.5:c.-82+25042A>C ENSP00000474863.1:n.-82+25042A>C
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