Canonical Allele Identifier: CA2729697978
Gene: FRMD6 HGNC NCBI

Linked Data

dbSNP Id: rs2139858598
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.51610281T>C , CM000676.2:g.51610281T>C GRCh38
NC_000014.8:g.52076999T>C , CM000676.1:g.52076999T>C GRCh37
NC_000014.7:g.51146749T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356218.8:c.-147+39871T>C ENSP00000348550.4:n.-147+39871T>C
ENST00000554745.1:n.278-33171T>C
ENST00000556137.5:n.508+39871T>C
NM_001042481.2:c.-147+39871T>C NP_001035946.1:n.-147+39871T>C
XM_011536423.1:c.-147+39871T>C XP_011534725.1:n.-147+39871T>C
XM_011536424.1:c.-147+39871T>C XP_011534726.1:n.-147+39871T>C
XM_024449472.1:c.-147+39871T>C XP_024305240.1:n.-147+39871T>C
XM_024449473.1:c.-146-79410T>C XP_024305241.1:n.-146-79410T>C
NM_001042481.3:c.-147+39871T>C NP_001035946.1:n.-147+39871T>C
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