Canonical Allele Identifier: CA867669813
Gene: FRMD3 HGNC NCBI

Linked Data

dbSNP Id: rs1363364491

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.83549153G>A , CM000671.2:g.83549153G>A GRCh38
NC_000009.11:g.86164068G>A , CM000671.1:g.86164068G>A GRCh37
NC_000009.10:g.85353888G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017014588.1:c.24+11017C>T XP_016870077.1:n.24+11017C>T
XM_024447487.1:c.-142+25757C>T XP_024303255.1:n.-142+25757C>T
XM_024447489.1:c.-142+25757C>T XP_024303257.1:n.-142+25757C>T