Canonical Allele Identifier: CA1206196015
Gene: FIRRM HGNC NCBI

Linked Data

dbSNP Id: rs1647462381

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000498289.5:n.518-1654A>G
XR_001738282.1:n.274-1577A>G