Canonical Allele Identifier: CA1206196049
Gene: FIRRM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169681855A= , CM000663.2:g.169681855A= GRCh38
NC_000001.10:g.169650996A= , CM000663.1:g.169650996A= GRCh37
NC_000001.9:g.167917620A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000498289.5:n.518-1614A=
XR_001738282.1:n.274-1537A=