Canonical Allele Identifier: CA867669886
Gene: FRMD3 HGNC NCBI

Linked Data

dbSNP Id: rs1338239880

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.83549287T>C , CM000671.2:g.83549287T>C GRCh38
NC_000009.11:g.86164202T>C , CM000671.1:g.86164202T>C GRCh37
NC_000009.10:g.85354022T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017014588.1:c.24+10883A>G XP_016870077.1:n.24+10883A>G
XM_024447487.1:c.-142+25623A>G XP_024303255.1:n.-142+25623A>G
XM_024447489.1:c.-142+25623A>G XP_024303257.1:n.-142+25623A>G