Canonical Allele Identifier: CA195349747
Gene: FRMD3 HGNC NCBI

Linked Data

dbSNP Id: rs970241251

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.83549085C>A , CM000671.2:g.83549085C>A GRCh38
NC_000009.11:g.86164000C>A , CM000671.1:g.86164000C>A GRCh37
NC_000009.10:g.85353820C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017014588.1:c.24+11085G>T XP_016870077.1:n.24+11085G>T
XM_024447487.1:c.-142+25825G>T XP_024303255.1:n.-142+25825G>T
XM_024447489.1:c.-142+25825G>T XP_024303257.1:n.-142+25825G>T