Canonical Allele Identifier: CA963110828
Gene: FRMD6 HGNC NCBI

Linked Data

dbSNP Id: rs546525267

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.51610404G>T , CM000676.2:g.51610404G>T GRCh38
NC_000014.8:g.52077122G>T , CM000676.1:g.52077122G>T GRCh37
NC_000014.7:g.51146872G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356218.8:c.-147+39994G>T ENSP00000348550.4:n.-147+39994G>T
ENST00000554745.1:n.278-33048G>T
ENST00000556137.5:n.508+39994G>T
NM_001042481.2:c.-147+39994G>T NP_001035946.1:n.-147+39994G>T
XM_011536423.1:c.-147+39994G>T XP_011534725.1:n.-147+39994G>T
XM_011536424.1:c.-147+39994G>T XP_011534726.1:n.-147+39994G>T
XM_024449472.1:c.-147+39994G>T XP_024305240.1:n.-147+39994G>T
XM_024449473.1:c.-146-79287G>T XP_024305241.1:n.-146-79287G>T
NM_001042481.3:c.-147+39994G>T NP_001035946.1:n.-147+39994G>T