Canonical Allele Identifier: CA1206196038
Gene: FIRRM HGNC NCBI

Linked Data

dbSNP Id: rs1647463030
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169681843C>G , CM000663.2:g.169681843C>G GRCh38
NC_000001.10:g.169650984C>G , CM000663.1:g.169650984C>G GRCh37
NC_000001.9:g.167917608C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000498289.5:n.518-1626C>G
XR_001738282.1:n.274-1549C>G
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