Canonical Allele Identifier: CA588976980
Gene: FRMD3 HGNC NCBI

Linked Data

dbSNP Id: rs1229005091
gnomAD v2: 9-86164175-C-T
gnomAD v3: 9-83549260-C-T
gnomAD v4: 9-83549260-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.83549260C>T , CM000671.2:g.83549260C>T GRCh38
NC_000009.11:g.86164175C>T , CM000671.1:g.86164175C>T GRCh37
NC_000009.10:g.85353995C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017014588.1:c.24+10910G>A XP_016870077.1:n.24+10910G>A
XM_024447487.1:c.-142+25650G>A XP_024303255.1:n.-142+25650G>A
XM_024447489.1:c.-142+25650G>A XP_024303257.1:n.-142+25650G>A