Canonical Allele Identifier: CA890964361
Gene: FIRRM HGNC NCBI

Linked Data

dbSNP Id: rs1355325012

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169681862G>C , CM000663.2:g.169681862G>C GRCh38
NC_000001.10:g.169651003G>C , CM000663.1:g.169651003G>C GRCh37
NC_000001.9:g.167917627G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000498289.5:n.518-1607G>C
XR_001738282.1:n.274-1530G>C