Canonical Allele Identifier: CA195349825
Gene: FRMD3 HGNC NCBI

Linked Data

dbSNP Id: rs927389705
gnomAD v2: 9-86164195-G-T
MyVariant Identifiers: chr9:g.86164195G>T (hg19) chr9:g.83549280G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.83549280G>T , CM000671.2:g.83549280G>T GRCh38
NC_000009.11:g.86164195G>T , CM000671.1:g.86164195G>T GRCh37
NC_000009.10:g.85354015G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017014588.1:c.24+10890C>A XP_016870077.1:n.24+10890C>A
XM_024447487.1:c.-142+25630C>A XP_024303255.1:n.-142+25630C>A
XM_024447489.1:c.-142+25630C>A XP_024303257.1:n.-142+25630C>A
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