Canonical Allele Identifier: CA662078841

Gene: FRMD4A

Linked Data

• dbSNP Id: rs1197783165
• MyVariant Identifiers: chr10:g.14478524G>C (hg19) ; chr10:g.14436525G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.14436525G>C , CM000672.2:g.14436525G>C	GRCh38
NC_000010.10:g.14478524G>C , CM000672.1:g.14478524G>C	GRCh37
NC_000010.9:g.14518530G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000475141.2:c.-305+25543C>G	ENSP00000473870.1:n.-305+25543C>G
ENST00000493380.5:c.-82+25543C>G	ENSP00000474863.1:n.-82+25543C>G