Canonical Allele Identifier: CA2548995122
Gene: FIRRM HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169681805C>T , CM000663.2:g.169681805C>T GRCh38
NC_000001.10:g.169650946C>T , CM000663.1:g.169650946C>T GRCh37
NC_000001.9:g.167917570C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000498289.5:n.518-1664C>T
XR_001738282.1:n.274-1587C>T
Search 100 bp 5'
Search 100 bp 3'