Canonical Allele Identifier: CA867669834

Gene: FRMD3

Linked Data

• dbSNP Id: rs1470495012
• gnomAD v3: 9-83549168-T-C
• gnomAD v4: 9-83549168-T-C
• MyVariant Identifiers: chr9:g.86164083T>C (hg19) ; chr9:g.83549168T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.83549168T>C , CM000671.2:g.83549168T>C	GRCh38
NC_000009.11:g.86164083T>C , CM000671.1:g.86164083T>C	GRCh37
NC_000009.10:g.85353903T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XM_017014588.1:c.24+11002A>G	XP_016870077.1:n.24+11002A>G
XM_024447487.1:c.-142+25742A>G	XP_024303255.1:n.-142+25742A>G
XM_024447489.1:c.-142+25742A>G	XP_024303257.1:n.-142+25742A>G