Canonical Allele Identifier: CA32442819

Gene: FIRRM

Linked Data

• dbSNP Id: rs1024836150
• gnomAD v3: 1-169681823-G-T
• gnomAD v4: 1-169681823-G-T
• MyVariant Identifiers: chr1:g.169650964G>T (hg19) ; chr1:g.169681823G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169681823G>T , CM000663.2:g.169681823G>T	GRCh38
NC_000001.10:g.169650964G>T , CM000663.1:g.169650964G>T	GRCh37
NC_000001.9:g.167917588G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000498289.5:n.518-1646G>T
XR_001738282.1:n.274-1569G>T