Canonical Allele Identifier: CA1860139929
Gene: FRMD3 HGNC NCBI

Linked Data

dbSNP Id: rs927389705

Genomic Alleles

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

Transcript Alleles

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