Canonical Allele Identifier: CA867669880
Gene: FRMD3 HGNC NCBI

Linked Data

dbSNP Id: rs553698489
gnomAD v3: 9-83549279-T-A
gnomAD v4: 9-83549279-T-A
MyVariant Identifiers: chr9:g.86164194T>A (hg19) chr9:g.83549279T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.83549279T>A , CM000671.2:g.83549279T>A GRCh38
NC_000009.11:g.86164194T>A , CM000671.1:g.86164194T>A GRCh37
NC_000009.10:g.85354014T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017014588.1:c.24+10891A>T XP_016870077.1:n.24+10891A>T
XM_024447487.1:c.-142+25631A>T XP_024303255.1:n.-142+25631A>T
XM_024447489.1:c.-142+25631A>T XP_024303257.1:n.-142+25631A>T
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