Canonical Allele Identifier: CA1008987986
Gene: FIRRM HGNC NCBI

Linked Data

dbSNP Id: rs1647462967
gnomAD v3: 1-169681840-A-G
gnomAD v4: 1-169681840-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169681840A>G , CM000663.2:g.169681840A>G GRCh38
NC_000001.10:g.169650981A>G , CM000663.1:g.169650981A>G GRCh37
NC_000001.9:g.167917605A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000498289.5:n.518-1629A>G
XR_001738282.1:n.274-1552A>G
Search 100 bp 5'
Search 100 bp 3'