Canonical Allele Identifier: CA867669782

Gene: FRMD3

Linked Data

• dbSNP Id: rs1261567949
• gnomAD v3: 9-83549123-G-T
• gnomAD v4: 9-83549123-G-T
• MyVariant Identifiers: chr9:g.86164038G>T (hg19) ; chr9:g.83549123G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.83549123G>T , CM000671.2:g.83549123G>T	GRCh38
NC_000009.11:g.86164038G>T , CM000671.1:g.86164038G>T	GRCh37
NC_000009.10:g.85353858G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_017014588.1:c.24+11047C>A	XP_016870077.1:n.24+11047C>A
XM_024447487.1:c.-142+25787C>A	XP_024303255.1:n.-142+25787C>A
XM_024447489.1:c.-142+25787C>A	XP_024303257.1:n.-142+25787C>A