Canonical Allele Identifier: CA588976976

Gene: FRMD3

Linked Data

• dbSNP Id: rs1296119771
• gnomAD v2: 9-86164150-A-G
• gnomAD v3: 9-83549235-A-G
• gnomAD v4: 9-83549235-A-G
• MyVariant Identifiers: chr9:g.86164150A>G (hg19) ; chr9:g.83549235A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.83549235A>G , CM000671.2:g.83549235A>G	GRCh38
NC_000009.11:g.86164150A>G , CM000671.1:g.86164150A>G	GRCh37
NC_000009.10:g.85353970A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XM_017014588.1:c.24+10935T>C	XP_016870077.1:n.24+10935T>C
XM_024447487.1:c.-142+25675T>C	XP_024303255.1:n.-142+25675T>C
XM_024447489.1:c.-142+25675T>C	XP_024303257.1:n.-142+25675T>C