Canonical Allele Identifier: CA1860139784
Gene: FRMD3 HGNC NCBI

Linked Data

dbSNP Id: rs1830096024

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.83549090C>T , CM000671.2:g.83549090C>T GRCh38
NC_000009.11:g.86164005C>T , CM000671.1:g.86164005C>T GRCh37
NC_000009.10:g.85353825C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017014588.1:c.24+11080G>A XP_016870077.1:n.24+11080G>A
XM_024447487.1:c.-142+25820G>A XP_024303255.1:n.-142+25820G>A
XM_024447489.1:c.-142+25820G>A XP_024303257.1:n.-142+25820G>A