Canonical Allele Identifier: CA1373171218

Gene: FRMD4B

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69393486G>T , CM000665.2:g.69393486G>T	GRCh38
NC_000003.11:g.69442637G>T , CM000665.1:g.69442637G>T	GRCh37
NC_000003.10:g.69525327G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000459638.5:c.-1+39148C>A	ENSP00000417550.1:n.-1+39148C>A
ENST00000497757.1:n.271+39148C>A
ENST00000497880.5:c.-1+39148C>A	ENSP00000417765.1:n.-1+39148C>A
XM_006713063.2:c.-1+39148C>A	XP_006713126.1:n.-1+39148C>A
XM_017005991.1:c.-1+39148C>A	XP_016861480.1:n.-1+39148C>A
XM_017005993.1:c.-1+39148C>A	XP_016861482.1:n.-1+39148C>A