Canonical Allele Identifier: CA1140140347
Community Standard Title: NC_000001.11:g.169681903G=
Gene: FIRRM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169681903G= , CM000663.2:g.169681903G= GRCh38
NC_000001.10:g.169651044G= , CM000663.1:g.169651044G= GRCh37
NC_000001.9:g.167917668G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000498289.5:n.518-1566G=
XR_001738282.1:n.274-1489G=