Canonical Allele Identifier: CA2746580898

Gene: FIRRM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169681856G>A , CM000663.2:g.169681856G>A	GRCh38
NC_000001.10:g.169650997G>A , CM000663.1:g.169650997G>A	GRCh37
NC_000001.9:g.167917621G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000498289.5:n.518-1613G>A
XR_001738282.1:n.274-1536G>A