Canonical Allele Identifier: CA588976966
Gene: FRMD3 HGNC NCBI

Linked Data

dbSNP Id: rs1187857950
gnomAD v2: 9-86163978-C-T
gnomAD v3: 9-83549063-C-T
gnomAD v4: 9-83549063-C-T
MyVariant Identifiers: chr9:g.86163978C>T (hg19) chr9:g.83549063C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.83549063C>T , CM000671.2:g.83549063C>T GRCh38
NC_000009.11:g.86163978C>T , CM000671.1:g.86163978C>T GRCh37
NC_000009.10:g.85353798C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017014588.1:c.24+11107G>A XP_016870077.1:n.24+11107G>A
XM_024447487.1:c.-142+25847G>A XP_024303255.1:n.-142+25847G>A
XM_024447489.1:c.-142+25847G>A XP_024303257.1:n.-142+25847G>A
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