Canonical Allele Identifier: CA1860139759
Gene: FRMD3 HGNC NCBI

Linked Data

dbSNP Id: rs1830095756

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.83549070C>A , CM000671.2:g.83549070C>A GRCh38
NC_000009.11:g.86163985C>A , CM000671.1:g.86163985C>A GRCh37
NC_000009.10:g.85353805C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017014588.1:c.24+11100G>T XP_016870077.1:n.24+11100G>T
XM_024447487.1:c.-142+25840G>T XP_024303255.1:n.-142+25840G>T
XM_024447489.1:c.-142+25840G>T XP_024303257.1:n.-142+25840G>T