Canonical Allele Identifier: CA5414996

Gene: FRMD4A

Linked Data

• dbSNP Id: rs774525698
• ExAC: 10:14478534 G / C
• gnomAD v2: 10-14478534-G-C
• gnomAD v3: 10-14436535-G-C
• gnomAD v4: 10-14436535-G-C
• MyVariant Identifiers: chr10:g.14478534G>C (hg19) ; chr10:g.14436535G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.14436535G>C , CM000672.2:g.14436535G>C	GRCh38
NC_000010.10:g.14478534G>C , CM000672.1:g.14478534G>C	GRCh37
NC_000010.9:g.14518540G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000475141.2:c.-305+25533C>G	ENSP00000473870.1:n.-305+25533C>G
ENST00000493380.5:c.-82+25533C>G	ENSP00000474863.1:n.-82+25533C>G