Canonical Allele Identifier: CA1860139921
Gene: FRMD3 HGNC NCBI

Linked Data

dbSNP Id: rs1830097945

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.83549274A>C , CM000671.2:g.83549274A>C GRCh38
NC_000009.11:g.86164189A>C , CM000671.1:g.86164189A>C GRCh37
NC_000009.10:g.85354009A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017014588.1:c.24+10896T>G XP_016870077.1:n.24+10896T>G
XM_024447487.1:c.-142+25636T>G XP_024303255.1:n.-142+25636T>G
XM_024447489.1:c.-142+25636T>G XP_024303257.1:n.-142+25636T>G