Canonical Allele Identifier: CA203745913

Gene: FRMD4A

Linked Data

• dbSNP Id: rs1021634717
• gnomAD v2: 10-14478549-G-A
• gnomAD v4: 10-14436550-G-A
• MyVariant Identifiers: chr10:g.14478549G>A (hg19) ; chr10:g.14436550G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.14436550G>A , CM000672.2:g.14436550G>A	GRCh38
NC_000010.10:g.14478549G>A , CM000672.1:g.14478549G>A	GRCh37
NC_000010.9:g.14518555G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000475141.2:c.-305+25518C>T	ENSP00000473870.1:n.-305+25518C>T
ENST00000493380.5:c.-82+25518C>T	ENSP00000474863.1:n.-82+25518C>T