Canonical Allele Identifier: CA1206196032
Gene: FIRRM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169681838A= , CM000663.2:g.169681838A= GRCh38
NC_000001.10:g.169650979A= , CM000663.1:g.169650979A= GRCh37
NC_000001.9:g.167917603A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000498289.5:n.518-1631A=
XR_001738282.1:n.274-1554A=