Canonical Allele Identifier: CA592244854

Gene: FRMD4A

Linked Data

• dbSNP Id: rs1296600438
• gnomAD v2: 10-14478680-A-C
• gnomAD v4: 10-14436681-A-C
• MyVariant Identifiers: chr10:g.14478680A>C (hg19) ; chr10:g.14436681A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.14436681A>C , CM000672.2:g.14436681A>C	GRCh38
NC_000010.10:g.14478680A>C , CM000672.1:g.14478680A>C	GRCh37
NC_000010.9:g.14518686A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475141.2:c.-305+25387T>G	ENSP00000473870.1:n.-305+25387T>G
ENST00000493380.5:c.-82+25387T>G	ENSP00000474863.1:n.-82+25387T>G