Canonical Allele Identifier: CA2136729458
Gene: FRMD6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.51610402T= , CM000676.2:g.51610402T= GRCh38
NC_000014.8:g.52077120T= , CM000676.1:g.52077120T= GRCh37
NC_000014.7:g.51146870T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356218.8:c.-147+39992T= ENSP00000348550.4:n.-147+39992T=
ENST00000554745.1:n.278-33050T=
ENST00000556137.5:n.508+39992T=
NM_001042481.2:c.-147+39992T= NP_001035946.1:n.-147+39992T=
XM_011536423.1:c.-147+39992T= XP_011534725.1:n.-147+39992T=
XM_011536424.1:c.-147+39992T= XP_011534726.1:n.-147+39992T=
XM_024449472.1:c.-147+39992T= XP_024305240.1:n.-147+39992T=
XM_024449473.1:c.-146-79289T= XP_024305241.1:n.-146-79289T=
NM_001042481.3:c.-147+39992T= NP_001035946.1:n.-147+39992T=