Canonical Allele Identifier: CA1206196045
Gene: FIRRM HGNC NCBI

Linked Data

dbSNP Id: rs1647463159

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169681846A>G , CM000663.2:g.169681846A>G GRCh38
NC_000001.10:g.169650987A>G , CM000663.1:g.169650987A>G GRCh37
NC_000001.9:g.167917611A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000498289.5:n.518-1623A>G
XR_001738282.1:n.274-1546A>G