Canonical Allele Identifier: CA1860139932
Gene: FRMD3 HGNC NCBI

Linked Data

dbSNP Id: rs1830098252

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.83549282T>C , CM000671.2:g.83549282T>C GRCh38
NC_000009.11:g.86164197T>C , CM000671.1:g.86164197T>C GRCh37
NC_000009.10:g.85354017T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017014588.1:c.24+10888A>G XP_016870077.1:n.24+10888A>G
XM_024447487.1:c.-142+25628A>G XP_024303255.1:n.-142+25628A>G
XM_024447489.1:c.-142+25628A>G XP_024303257.1:n.-142+25628A>G