Canonical Allele Identifier: CA2136729335
Gene: FRMD6 HGNC NCBI

Linked Data

dbSNP Id: rs1566501143

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.51610311C>T , CM000676.2:g.51610311C>T GRCh38
NC_000014.8:g.52077029C>T , CM000676.1:g.52077029C>T GRCh37
NC_000014.7:g.51146779C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356218.8:c.-147+39901C>T ENSP00000348550.4:n.-147+39901C>T
ENST00000554745.1:n.278-33141C>T
ENST00000556137.5:n.508+39901C>T
NM_001042481.2:c.-147+39901C>T NP_001035946.1:n.-147+39901C>T
XM_011536423.1:c.-147+39901C>T XP_011534725.1:n.-147+39901C>T
XM_011536424.1:c.-147+39901C>T XP_011534726.1:n.-147+39901C>T
XM_024449472.1:c.-147+39901C>T XP_024305240.1:n.-147+39901C>T
XM_024449473.1:c.-146-79380C>T XP_024305241.1:n.-146-79380C>T
NM_001042481.3:c.-147+39901C>T NP_001035946.1:n.-147+39901C>T