Canonical Allele Identifier: CA1206196017
Gene: FIRRM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169681815A= , CM000663.2:g.169681815A= GRCh38
NC_000001.10:g.169650956A= , CM000663.1:g.169650956A= GRCh37
NC_000001.9:g.167917580A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000498289.5:n.518-1654A=
XR_001738282.1:n.274-1577A=