Canonical Allele Identifier: CA1860139831

Gene: FRMD3

Linked Data

• dbSNP Id: rs1830096685

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.83549144C>G , CM000671.2:g.83549144C>G	GRCh38
NC_000009.11:g.86164059C>G , CM000671.1:g.86164059C>G	GRCh37
NC_000009.10:g.85353879C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XM_017014588.1:c.24+11026G>C	XP_016870077.1:n.24+11026G>C
XM_024447487.1:c.-142+25766G>C	XP_024303255.1:n.-142+25766G>C
XM_024447489.1:c.-142+25766G>C	XP_024303257.1:n.-142+25766G>C