Canonical Allele Identifier: CA1860139822

Gene: FRMD3

Linked Data

• dbSNP Id: rs1830096543

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.83549135T>C , CM000671.2:g.83549135T>C	GRCh38
NC_000009.11:g.86164050T>C , CM000671.1:g.86164050T>C	GRCh37
NC_000009.10:g.85353870T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XM_017014588.1:c.24+11035A>G	XP_016870077.1:n.24+11035A>G
XM_024447487.1:c.-142+25775A>G	XP_024303255.1:n.-142+25775A>G
XM_024447489.1:c.-142+25775A>G	XP_024303257.1:n.-142+25775A>G