Canonical Allele Identifier: CA2697442568
Gene: FIRRM HGNC NCBI

Linked Data

dbSNP Id: rs2101966220

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169681835T>C , CM000663.2:g.169681835T>C GRCh38
NC_000001.10:g.169650976T>C , CM000663.1:g.169650976T>C GRCh37
NC_000001.9:g.167917600T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000498289.5:n.518-1634T>C
XR_001738282.1:n.274-1557T>C