Canonical Allele Identifier: CA867669777
Gene: FRMD3 HGNC NCBI

Linked Data

dbSNP Id: rs1481089510
gnomAD v3: 9-83549073-G-C
gnomAD v4: 9-83549073-G-C
MyVariant Identifiers: chr9:g.86163988G>C (hg19) chr9:g.83549073G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.83549073G>C , CM000671.2:g.83549073G>C GRCh38
NC_000009.11:g.86163988G>C , CM000671.1:g.86163988G>C GRCh37
NC_000009.10:g.85353808G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017014588.1:c.24+11097C>G XP_016870077.1:n.24+11097C>G
XM_024447487.1:c.-142+25837C>G XP_024303255.1:n.-142+25837C>G
XM_024447489.1:c.-142+25837C>G XP_024303257.1:n.-142+25837C>G
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