Canonical Allele Identifier: CA867669874
Gene: FRMD3 HGNC NCBI

Linked Data

dbSNP Id: rs1250695333

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.83549260del , CM000671.2:g.83549260del GRCh38
NC_000009.11:g.86164175del , CM000671.1:g.86164175del GRCh37
NC_000009.10:g.85353995del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017014588.1:c.24+10911del XP_016870077.1:n.24+10911del
XM_024447487.1:c.-142+25651del XP_024303255.1:n.-142+25651del
XM_024447489.1:c.-142+25651del XP_024303257.1:n.-142+25651del