Canonical Allele Identifier: CA867669799

Gene: FRMD3

Linked Data

• dbSNP Id: rs1346124637
• gnomAD v3: 9-83549134-C-T
• gnomAD v4: 9-83549134-C-T
• MyVariant Identifiers: chr9:g.86164049C>T (hg19) ; chr9:g.83549134C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.83549134C>T , CM000671.2:g.83549134C>T	GRCh38
NC_000009.11:g.86164049C>T , CM000671.1:g.86164049C>T	GRCh37
NC_000009.10:g.85353869C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_017014588.1:c.24+11036G>A	XP_016870077.1:n.24+11036G>A
XM_024447487.1:c.-142+25776G>A	XP_024303255.1:n.-142+25776G>A
XM_024447489.1:c.-142+25776G>A	XP_024303257.1:n.-142+25776G>A