Canonical Allele Identifier: CA890964356

Gene: FIRRM

Linked Data

• dbSNP Id: rs765680534
• gnomAD v3: 1-169681826-A-G
• gnomAD v4: 1-169681826-A-G
• MyVariant Identifiers: chr1:g.169650967A>G (hg19) ; chr1:g.169681826A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169681826A>G , CM000663.2:g.169681826A>G	GRCh38
NC_000001.10:g.169650967A>G , CM000663.1:g.169650967A>G	GRCh37
NC_000001.9:g.167917591A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000498289.5:n.518-1643A>G
XR_001738282.1:n.274-1566A>G