Canonical Allele Identifier: CA592244580

Gene: FRMD4A

Linked Data

• dbSNP Id: rs1244750857
• gnomAD v2: 10-14478567-A-G
• gnomAD v4: 10-14436568-A-G
• MyVariant Identifiers: chr10:g.14478567A>G (hg19) ; chr10:g.14436568A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.14436568A>G , CM000672.2:g.14436568A>G	GRCh38
NC_000010.10:g.14478567A>G , CM000672.1:g.14478567A>G	GRCh37
NC_000010.9:g.14518573A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000475141.2:c.-305+25500T>C	ENSP00000473870.1:n.-305+25500T>C
ENST00000493380.5:c.-82+25500T>C	ENSP00000474863.1:n.-82+25500T>C