Canonical Allele Identifier: CA1206196047
Gene: FIRRM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169681850C= , CM000663.2:g.169681850C= GRCh38
NC_000001.10:g.169650991C= , CM000663.1:g.169650991C= GRCh37
NC_000001.9:g.167917615C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000498289.5:n.518-1619C=
XR_001738282.1:n.274-1542C=